A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609035



Internal ID16049758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:151199137..151258679hg38UCSC Ensembl
Innerchr7:150896223..150955765hg19UCSC Ensembl
Innerchr7:150527156..150586698hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3859543
hg1959543
hg1859543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1099590
Samples
Known GenesABCF2, CHPF2, MIR671, SMARCD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609035
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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