A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608075



Internal ID16395484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108952167..109017662hg38UCSC Ensembl
Innerchr7:108592224..108657719hg19UCSC Ensembl
Innerchr7:108379460..108444955hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3865496
hg1965496
hg1865496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092082
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608075
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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