A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605826



Internal ID16046549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1640529..1717600hg38UCSC Ensembl
Innerchr7:1680165..1757236hg19UCSC Ensembl
Innerchr7:1646691..1723762hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3877072
hg1977072
hg1877072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078364
Samples
Known GenesELFN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605826
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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