A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099596



Internal ID15606096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152296623..152373073hg38UCSC Ensembl
Innerchr7:151993708..152070158hg19UCSC Ensembl
Innerchr7:151624641..151701091hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3876451
hg1976451
hg1876451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609047
Supporting Variants
Samples
Known GenesKMT2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1099596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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