A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064105



Internal ID18806636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55808050..55939166hg38UCSC Ensembl
Innerchr19:56319416..56450532hg19UCSC Ensembl
Innerchr19:61011228..61142344hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38131117
hg19131117
hg18131117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570438
Samples
Known GenesNLRP11, NLRP13, NLRP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064105
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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