A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3500981



Internal ID18741936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2649384..3089361hg38UCSC Ensembl
Innerchr10:2691576..3131553hg19UCSC Ensembl
Innerchr10:2681576..3121553hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38439978
hg19439978
hg18439978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052921
Supporting Variants
Samples
Known GenesPFKP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3500981
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