A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703085



Internal ID15093051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150932060..150952038hg38UCSC Ensembl
Innerchr5:150311622..150331600hg19UCSC Ensembl
Innerchr5:150291815..150311793hg18UCSC Ensembl
Innerchr5:150291815..150311793hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3819979
hg1919979
hg1819979
hg1719979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526742
Supporting Variants
Samples
Known GenesZNF300P1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703085
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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