A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135845



Internal ID18933282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79739737..79740141hg38UCSC Ensembl
Outerchr18:77499737..77500141hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1661n106
Supporting Variantsnssv3989437
SamplesKWS2
Known GenesCTDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135845
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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