A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674856



Internal ID15064822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60398877..61107733hg38UCSC Ensembl
Innerchr6:57370914..58075480hg19UCSC Ensembl
Innerchr6:57478873..58183439hg18UCSC Ensembl
Innerchr6:57478873..58183439hg17UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38708857
hg19704567
hg18704567
hg17704567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515916
Supporting Variants
Samples
Known GenesPRIM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674856
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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