A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662417



Internal ID15052383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152338225..152424360hg38UCSC Ensembl
Innerchr7:152035310..152121445hg19UCSC Ensembl
Innerchr7:151666243..151752378hg18UCSC Ensembl
Innerchr7:151472958..151559093hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3886136
hg1986136
hg1886136
hg1786136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517255
Supporting Variants
Samples
Known GenesKMT2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662417
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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