A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029882



Internal ID18772413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10832535..11331518hg38UCSC Ensembl
Innerchr7:10872162..11371145hg19UCSC Ensembl
Innerchr7:10838687..11337670hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38498984
hg19498984
hg18498984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642917
Samples
Known GenesNDUFA4, PHF14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029882
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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