A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999845



Internal ID16946111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:41878331..41881433hg38UCSC Ensembl
Outerchr19:42382401..42385500hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383103
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953579
Supporting Variants
SamplesBILGI_BIOE
Known GenesCD79A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999845
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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