A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706008



Internal ID15095974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152145880..152147402hg38UCSC Ensembl
Innerchr7:151842965..151844487hg19UCSC Ensembl
Innerchr7:151473898..151475420hg18UCSC Ensembl
Innerchr7:151280613..151282135hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381523
hg191523
hg181523
hg171523
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522613
Supporting Variants
Samples
Known GenesKMT2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706008
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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