A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037411



Internal ID19126630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72041367..72056009hg38UCSC Ensembl
Innerchr10:73801125..73815767hg19UCSC Ensembl
Innerchr10:73471131..73485773hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3814643
hg1914643
hg1814643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505332, nssv3503685
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)nsv1037411
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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