A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079013



Internal ID15932199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8644051..8796226hg38UCSC Ensembl
Innerchr7:8683681..8835856hg19UCSC Ensembl
Innerchr7:8650206..8802381hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38152176
hg19152176
hg18152176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606090
Supporting Variants
Samples
Known GenesNXPH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079013
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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