A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063523



Internal ID19152742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53519155..53597032hg38UCSC Ensembl
Innerchr19:54022409..54100286hg19UCSC Ensembl
Innerchr19:58714221..58792098hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3877878
hg1977878
hg1877878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726549
Samples
Known GenesZNF331
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063523
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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