A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573421



Internal ID18525016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54297012..54587836hg38UCSC Ensembl
Innerchr19:54805518..55099303hg19UCSC Ensembl
Innerchr19:59497330..59791115hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38290825
hg19293786
hg18293786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059816
Supporting Variants
Samples
Known GenesCDC42EP5, KIR3DX1, LAIR1, LAIR2, LENG8, LENG9, LILRA2, LILRA4, LILRA5, TTYH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573421
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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