A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061761



Internal ID18804292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29964373..29988391hg38UCSC Ensembl
Innerchr19:30455280..30479298hg19UCSC Ensembl
Innerchr19:35147120..35171138hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3824019
hg1924019
hg1824019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3511n100
Supporting Variantsnssv3566545
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061761
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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