A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657052



Internal ID18955333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76811864..77109291hg38UCSC Ensembl
Innerchr7:76441181..76738608hg19UCSC Ensembl
Innerchr7:76279117..76576544hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38297428
hg19297428
hg18297428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019630
Supporting Variants
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100132832
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657052
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