A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661949



Internal ID18960230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62720720..63332411hg38UCSC Ensembl
Innerchr7:62181098..62792789hg19UCSC Ensembl
Innerchr7:61818533..62430224hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38611692
hg19611692
hg18611692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027893
Supporting Variants
Samples
Known GenesZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661949
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