A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062561



Internal ID18805092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57622557..57647522hg38UCSC Ensembl
Innerchr19:58133925..58158890hg19UCSC Ensembl
Innerchr19:62825737..62850702hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3824966
hg1924966
hg1824966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3685n100
Supporting Variantsnssv3570455, nssv3726651
Samples
Known GenesZNF211
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062561
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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