A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673658



Internal ID15063624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152338225..152373073hg38UCSC Ensembl
Innerchr7:152035310..152070158hg19UCSC Ensembl
Innerchr7:151666243..151701091hg18UCSC Ensembl
Innerchr7:151472958..151507806hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3834849
hg1934849
hg1834849
hg1734849
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)nssv673658
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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