A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057367



Internal ID18799898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11920972..11950569hg38UCSC Ensembl
Innerchr19:12031787..12061384hg19UCSC Ensembl
Innerchr19:11892787..11922384hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3829598
hg1929598
hg1829598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3429n100
Supporting Variantsnssv3564700
Samples
Known GenesZNF700
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057367
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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