A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724919



Internal ID19023200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52434878..52537866hg38UCSC Ensembl
Innerchr19:52938131..53041119hg19UCSC Ensembl
Innerchr19:57629943..57732931hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38102989
hg19102989
hg18102989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063648
Supporting Variants
Samples
Known GenesZNF534, ZNF578, ZNF808
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3724919
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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