A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620481



Internal ID7007352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42830430..42870611hg38UCSC Ensembl
chr9:44100508..44140689hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3840182
hg1940182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13482428, essv13482426, essv13482421, essv13482420, essv13482424, essv13482419, essv13482423, essv13482429, essv13482422, essv13482427, essv13482425
SamplesHG01054, HG02262, NA12058, HG00641, HG02703, NA19189, HG01603, NA19707, HG03713, HG01111, NA18740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620481
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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