A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704214



Internal ID15440866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37920233..37934143hg38UCSC Ensembl
Innerchr9:37920230..37934140hg19UCSC Ensembl
Innerchr9:37910230..37924140hg18UCSC Ensembl
Innerchr9:37910230..37924140hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3813911
hg1913911
hg1813911
hg1713911
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527731
Supporting Variants
Samples
Known GenesSHB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704214
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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