A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645211



Internal ID18943492
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 StatusS
Merged Variantsnsv1024052
Supporting Variants
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)nssv3645211
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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