A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021311



Internal ID19110528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10577783..10613017hg38UCSC Ensembl
Innerchr5:10577895..10613129hg19UCSC Ensembl
Innerchr5:10630895..10666129hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3835235
hg1935235
hg1835235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638198
Samples
Known GenesANKRD33B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021311
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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