A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037173



Internal ID18779704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2641472..3089361hg38UCSC Ensembl
Innerchr10:2683664..3131553hg19UCSC Ensembl
Innerchr10:2673664..3121553hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38447890
hg19447890
hg18447890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv660n100
Supporting Variantsnssv3484439
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)nsv1037173
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