A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661777



Internal ID9927882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56670830..56672372hg38UCSC Ensembl
chr4:57536996..57538538hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381543
hg191543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5758808, essv5825584, essv5979483, essv5497361, essv6220146, essv6592897, essv6412602
SamplesNA19394, NA19701, NA18504, NA19190, NA19396, NA19404, NA19380
Known GenesHOPX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661777
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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