A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13514280



Internal ID3837407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71837148..71841711hg38UCSC Ensembl
Innerchr9:71837183..71841677hg38UCSC Ensembl
Outerchr9:71837114..71841746hg38UCSC Ensembl
chr9:74452064..74456627hg19UCSC Ensembl
Innerchr9:74452099..74456593hg19UCSC Ensembl
Outerchr9:74452030..74456662hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384564
hg194564
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620616
Supporting Variants
SamplesHG03472
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13514280
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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