A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055825



Internal ID19145044
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 StatusM
Merged Variantsdgv3627n100
Supporting Variantsnssv3724922
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)nsv1055825
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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