A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3991203



Internal ID18883042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:32727958..32728018hg38UCSC Ensembl
Outerchr18:30307921..30307981hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138618
Supporting Variants
SamplesKWS2
Known GenesKLHL14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3991203
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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