A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505362



Internal ID18803643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25048663..25109190hg38UCSC Ensembl
Innerchr10:25337592..25398119hg19UCSC Ensembl
Innerchr10:25377598..25438125hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3860528
hg1960528
hg1860528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036683
Supporting Variants
Samples
Known GenesENKUR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505362
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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