A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724922



Internal ID19023203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52498046..52534125hg38UCSC Ensembl
Innerchr19:53001299..53037378hg19UCSC Ensembl
Innerchr19:57693111..57729190hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3836080
hg1936080
hg1836080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055825
Supporting Variants
Samples
Known GenesZNF578, ZNF808
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3724922
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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