A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664248



Internal ID18962529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140212555..140287881hg38UCSC Ensembl
Innerchr7:139912355..139987681hg19UCSC Ensembl
Innerchr7:139558824..139634150hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3875327
hg1975327
hg1875327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015840
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)nssv3664248
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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