A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065558



Internal ID18808089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:305266..441626hg38UCSC Ensembl
Innerchr19:305266..441626hg19UCSC Ensembl
Innerchr19:256266..392626hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38136361
hg19136361
hg18136361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564595
Samples
Known GenesC2CD4C, MIER2, SHC2, THEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065558
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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