A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606624



Internal ID16394033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38028121..38084065hg38UCSC Ensembl
Innerchr7:38067723..38123667hg19UCSC Ensembl
Innerchr7:38034248..38090192hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3855945
hg1955945
hg1855945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1082704
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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