A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655292



Internal ID18953573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97766136..97793614hg38UCSC Ensembl
Innerchr7:97395448..97422926hg19UCSC Ensembl
Innerchr7:97233384..97260862hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3827479
hg1927479
hg1827479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017302
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)nssv3655292
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