A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681658



Internal ID15071624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65046526..65737334hg38UCSC Ensembl
Innerchr7:64506904..65202326hg19UCSC Ensembl
Innerchr7:64144339..64839761hg18UCSC Ensembl
Innerchr7:63951054..64646476hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38690809
hg19695423
hg18695423
hg17695423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517778
Supporting Variants
Samples
Known GenesCCT6P3, INTS4L2, LOC441242, ZNF92
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681658
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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