A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664832



Internal ID15054798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177432847..177458498hg38UCSC Ensembl
Innerchr5:176859848..176885499hg19UCSC Ensembl
Innerchr5:176792454..176818105hg18UCSC Ensembl
Innerchr5:176792454..176818105hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3825652
hg1925652
hg1825652
hg1725652
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515805
Supporting Variants
Samples
Known GenesDBN1, GRK6, PRR7, PRR7-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664832
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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