A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662501



Internal ID15399153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:92635679..92650049hg38UCSC Ensembl
Innerchr7:92264993..92279363hg19UCSC Ensembl
Innerchr7:92102929..92117299hg18UCSC Ensembl
Innerchr7:91909644..91924014hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3814371
hg1914371
hg1814371
hg1714371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516592
Supporting Variants
Samples
Known GenesCDK6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662501
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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