A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953941



Internal ID16956128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1205602..1322401hg38UCSC Ensembl
Outerchr19:1205601..1322400hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38116800
hg19116800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998920
SamplesBILGI_BIOE
Known GenesATP5D, C19orf24, C19orf26, CIRBP, CIRBP-AS1, EFNA2, MIDN, STK11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953941
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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