A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111955



Internal ID19255125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26991656..26992377hg38UCSC Ensembl
Outerchr18:24571620..24572341hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1569n106
Supporting Variantsnssv3964406, nssv3971180
SamplesKWS2, KWS1
Known GenesCHST9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111955
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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