A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606623



Internal ID16394032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37820873..37856656hg38UCSC Ensembl
Innerchr7:37860475..37896258hg19UCSC Ensembl
Innerchr7:37827000..37862783hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3835784
hg1935784
hg1835784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1082703
Samples
Known GenesNME8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606623
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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