A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056134



Internal ID19145353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36531137..36566041hg38UCSC Ensembl
Innerchr19:37022039..37056943hg19UCSC Ensembl
Innerchr19:41713879..41748783hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3834905
hg1934905
hg1834905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568187
Samples
Known GenesZNF529
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056134
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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