A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621814



Internal ID7008680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128759239..128767248hg38UCSC Ensembl
Innerchr9:128759739..128766748hg38UCSC Ensembl
Outerchr9:128758239..128768248hg38UCSC Ensembl
chr9:131521518..131529527hg19UCSC Ensembl
Innerchr9:131522018..131529027hg19UCSC Ensembl
Outerchr9:131520518..131530527hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg388010
hg198010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1510e214
Supporting Variantsessv13624967
SamplesHG02613
Known GenesZER1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621814
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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