A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999823



Internal ID17292775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35931899..35944598hg38UCSC Ensembl
Outerchr19:36422801..36435500hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812700
hg1912700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953287
Supporting Variants
SamplesBILGI_BIOE
Known GenesLRFN3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999823
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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