A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079014



Internal ID15932200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8644051..8798213hg38UCSC Ensembl
Innerchr7:8683681..8837843hg19UCSC Ensembl
Innerchr7:8650206..8804368hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38154163
hg19154163
hg18154163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606091
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)nssv1079014
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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