A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609049



Internal ID16049772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152316933..152361056hg38UCSC Ensembl
Innerchr7:152014018..152058141hg19UCSC Ensembl
Innerchr7:151644951..151689074hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3844124
hg1944124
hg1844124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1099598
Samples
Known GenesKMT2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609049
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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