A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035234



Internal ID19124453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8390076..8467715hg38UCSC Ensembl
Innerchr10:8432039..8509678hg19UCSC Ensembl
Innerchr10:8472045..8549684hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3877640
hg1977640
hg1877640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3483212
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)nsv1035234
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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