A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111921



Internal ID19259836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:75054235..75058816hg38UCSC Ensembl
Outerchr14:75520938..75525519hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384582
hg194582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1103n106
Supporting Variantsnssv3964833
SamplesKWS2
Known GenesACYP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111921
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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