A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981984



Internal ID19211923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:54101640..54102340hg38UCSC Ensembl
Outerchr8:55014200..55014900hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119178
Supporting Variants
SamplesKWS1
Known GenesLYPLA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981984
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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