A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061250



Internal ID19150469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36643166..36697869hg38UCSC Ensembl
Innerchr19:37134068..37188771hg19UCSC Ensembl
Innerchr19:41825908..41880611hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3854704
hg1954704
hg1854704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568188
Samples
Known GenesZNF461, ZNF567
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061250
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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