A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660908



Internal ID15397560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153501601..153544908hg38UCSC Ensembl
Innerchr6:153822736..153866043hg19UCSC Ensembl
Innerchr6:153864429..153907736hg18UCSC Ensembl
Innerchr6:153914850..153958157hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3843308
hg1943308
hg1843308
hg1743308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520116
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660908
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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