A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695213



Internal ID15431865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123099462..123110619hg38UCSC Ensembl
Innerchr9:125861741..125872898hg19UCSC Ensembl
Innerchr9:124901562..124912719hg18UCSC Ensembl
Innerchr9:122941295..122952452hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3811158
hg1911158
hg1811158
hg1711158
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517807
Supporting Variants
Samples
Known GenesMIR600HG, RABGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695213
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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