A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052321



Internal ID19141540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57503097..57592682hg38UCSC Ensembl
Innerchr10:59262857..59352442hg19UCSC Ensembl
Innerchr10:58932863..59022448hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3889586
hg1989586
hg1889586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv875n100
Supporting Variantsnssv3519143
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)nsv1052321
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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