A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573782



Internal ID18872063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44390001..44426631hg38UCSC Ensembl
Innerchr19:44894164..44930803hg19UCSC Ensembl
Innerchr19:49586004..49622643hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3836631
hg1936640
hg1836640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065783
Supporting Variants
Samples
Known GenesZNF229, ZNF285
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573782
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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