A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003986



Internal ID18840589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:80186299..80186578hg38UCSC Ensembl
Outerchr18:77944182..77944461hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151423
Supporting Variants
SamplesKWB1
Known GenesPARD6G
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003986
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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