A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024052



Internal ID19113269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110295110..110486388hg38UCSC Ensembl
Innerchr7:109935167..110126445hg19UCSC Ensembl
Innerchr7:109722403..109913681hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38191279
hg19191279
hg18191279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645211
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024052
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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