A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037610



Internal ID18780141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101373124..101579801hg38UCSC Ensembl
Innerchr10:103132881..103339558hg19UCSC Ensembl
Innerchr10:103122871..103329548hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38206678
hg19206678
hg18206678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv964n100
Supporting Variantsnssv3505154
Samples
Known GenesBTRC, POLL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037610
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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