A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674663



Internal ID18626258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154832424..154947546hg38UCSC Ensembl
Innerchr7:154624134..154739256hg19UCSC Ensembl
Innerchr7:154255067..154370189hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38115123
hg19115123
hg18115123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033085
Supporting Variants
Samples
Known GenesDPP6, PAXIP1, PAXIP1-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674663
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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