A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515805



Internal ID15096412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177432847..177469411hg38UCSC Ensembl
Innerchr5:176859848..176896412hg19UCSC Ensembl
Innerchr5:176792454..176829018hg18UCSC Ensembl
Innerchr5:176792454..176829018hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3836565
hg1936565
hg1836565
hg1736565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684839, nssv700617, nssv664832, nssv661523
Samples
Known GenesDBN1, GRK6, PRR7, PRR7-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515805
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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