A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979030



Internal ID18862913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79739839..79740226hg38UCSC Ensembl
Outerchr18:77499839..77500226hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140319
Supporting Variants
SamplesKWS1
Known GenesCTDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979030
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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