A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605856



Internal ID16393265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1999959..2075768hg38UCSC Ensembl
Innerchr7:2039594..2115403hg19UCSC Ensembl
Innerchr7:2006120..2081929hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3875810
hg1975810
hg1875810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11143n54
Supporting Variantsnssv1155108
SamplesHGDP00787
Known GenesMAD1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605856
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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