A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607016



Internal ID16394425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53400030..53522557hg38UCSC Ensembl
Innerchr7:53467723..53590250hg19UCSC Ensembl
Innerchr7:53435217..53557744hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38122528
hg19122528
hg18122528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11348n54
Supporting Variantsnssv1154947, nssv1154948
SamplesHGDP00738, HGDP00643
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607016
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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