A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169663



Internal ID21313474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31511569..31521415hg38UCSC Ensembl
Outerchr19:31510261..31524632hg38UCSC Ensembl
Innerchr19:32002475..32012321hg19UCSC Ensembl
Outerchr19:32001167..32015538hg19UCSC Ensembl
Innerchr19:36694315..36704161hg18UCSC Ensembl
Outerchr19:36693007..36707378hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3814372
hg1914372
hg1814372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242739
SamplesSNI_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169663
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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