A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655633



Internal ID18953914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67796539..67922411hg38UCSC Ensembl
Innerchr7:67261526..67387398hg19UCSC Ensembl
Innerchr7:66898961..67024833hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38125873
hg19125873
hg18125873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027532
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)nssv3655633
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer