A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703629



Internal ID15440281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101608755..101609454hg38UCSC Ensembl
Innerchr9:104371037..104371736hg19UCSC Ensembl
Innerchr9:103410858..103411557hg18UCSC Ensembl
Innerchr9:101450592..101451291hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38700
hg19700
hg18700
hg17700
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527229
Supporting Variants
Samples
Known GenesGRIN3A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703629
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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