A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620120



Internal ID7006993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26889663..26890789hg38UCSC Ensembl
Innerchr9:26889707..26890746hg38UCSC Ensembl
Outerchr9:26889620..26890833hg38UCSC Ensembl
chr9:26889661..26890787hg19UCSC Ensembl
Innerchr9:26889705..26890744hg19UCSC Ensembl
Outerchr9:26889618..26890831hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13433595, essv13433598, essv13433596, essv13433597, essv13433600, essv13433599
SamplesNA20339, NA20294, HG02721, NA19323, HG03063, HG03258
Known GenesCAAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620120
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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