A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037340



Internal ID19126559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56569449..56721030hg38UCSC Ensembl
Innerchr10:58329209..58480790hg19UCSC Ensembl
Innerchr10:57999215..58150796hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38151582
hg19151582
hg18151582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869n100
Supporting Variantsnssv3504921
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)nsv1037340
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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