A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726653



Internal ID18678248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58229804..58349308hg38UCSC Ensembl
Innerchr19:58741170..58860674hg19UCSC Ensembl
Innerchr19:63432982..63552486hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38119505
hg19119505
hg18119505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058109
Supporting Variants
Samples
Known GenesA1BG, MIR6806, ZNF544, ZNF8, ZSCAN22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726653
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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