A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607925



Internal ID16395334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99157649..99190966hg38UCSC Ensembl
Innerchr7:98755272..98788589hg19UCSC Ensembl
Innerchr7:98593208..98626525hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3833318
hg1933318
hg1833318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154973, nssv1156552
SamplesHGDP01412, HGDP01418
Known GenesKPNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607925
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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