A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039892



Internal ID19129111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9480772..9660846hg38UCSC Ensembl
Innerchr10:9522735..9702809hg19UCSC Ensembl
Innerchr10:9562741..9742815hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38180075
hg19180075
hg18180075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n100
Supporting Variantsnssv3499142
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)nsv1039892
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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