A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041024



Internal ID19130243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3186413..3532212hg38UCSC Ensembl
Innerchr10:3228605..3574404hg19UCSC Ensembl
Innerchr10:3218605..3564404hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38345800
hg19345800
hg18345800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486721
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041024
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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