A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525777



Internal ID15453070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5181467..5292257hg38UCSC Ensembl
Innerchr9:5181467..5292257hg19UCSC Ensembl
Innerchr9:5171467..5282257hg18UCSC Ensembl
Innerchr9:5171467..5282257hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38110791
hg19110791
hg18110791
hg17110791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701950
Samples
Known GenesINSL4, INSL6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525777
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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