A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667435



Internal ID15057401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152338225..152425837hg38UCSC Ensembl
Innerchr7:152035310..152122922hg19UCSC Ensembl
Innerchr7:151666243..151753855hg18UCSC Ensembl
Innerchr7:151472958..151560570hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3887613
hg1987613
hg1887613
hg1787613
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)nssv667435
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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