A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064342



Internal ID19153561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52493457..52537866hg38UCSC Ensembl
Innerchr19:52996710..53041119hg19UCSC Ensembl
Innerchr19:57688522..57732931hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3844410
hg1944410
hg1844410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3627n100
Supporting Variantsnssv3724921
Samples
Known GenesZNF578, ZNF808
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064342
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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