A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605816



Internal ID16393225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1408552..1458126hg38UCSC Ensembl
Innerchr7:1448188..1497762hg19UCSC Ensembl
Innerchr7:1414714..1464288hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3849575
hg1949575
hg1849575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078354
Samples
Known GenesMICALL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605816
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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