A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609052



Internal ID16049775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152330539..152373073hg38UCSC Ensembl
Innerchr7:152027624..152070158hg19UCSC Ensembl
Innerchr7:151658557..151701091hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3842535
hg1942535
hg1842535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11729n54
Supporting Variantsnssv1155708
SamplesNINDS_7
Known GenesKMT2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609052
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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