A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042170



Internal ID19131389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114695284..114745112hg38UCSC Ensembl
Innerchr10:116455043..116504871hg19UCSC Ensembl
Innerchr10:116445033..116494861hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3849829
hg1949829
hg1849829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv976n100
Supporting Variantsnssv3506441
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)nsv1042170
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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