A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673885



Internal ID9939990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45207616..45208707hg38UCSC Ensembl
chr4:45209633..45210724hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381092
hg191092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6052877, essv5416519, essv5450399, essv5846403, essv5795193, essv6071348, essv5898298, essv5731098, essv6253085, essv5433139, essv6206552, essv5725324, essv6090315, essv5814501, essv5788925, essv5472154, essv6521815, essv5956033, essv5498010, essv6511077, essv6340924, essv5684298, essv5954240, essv6087045, essv6545555, essv5650016, essv5410105, essv6157220, essv6411653, essv6157152, essv6210829, essv6072009
SamplesNA19466, NA18917, NA19350, NA18870, NA18519, NA18874, NA19172, HG01198, NA18908, NA18867, NA19455, NA19236, NA19449, NA18856, NA18523, NA19318, NA19395, NA19434, NA19444, NA19835, NA19818, NA19376, NA19398, NA19223, NA19468, NA19713, NA19430, HG01082, NA20322, NA18511, NA18522, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673885
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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