A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6077991



Internal ID9165771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44791958..44793597hg38UCSC Ensembl
chr1:45257630..45259269hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381640
hg191640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668995
Supporting Variants
SamplesHG01365
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6077991
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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