A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665717



Internal ID15055683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17553782..17699091hg38UCSC Ensembl
Innerchr6:17554013..17699322hg19UCSC Ensembl
Innerchr6:17661992..17807301hg18UCSC Ensembl
Innerchr6:17661992..17807301hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38145310
hg19145310
hg18145310
hg17145310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516012
Supporting Variants
Samples
Known GenesCAP2, FAM8A1, NUP153
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665717
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