A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118282



Internal ID19275214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:73529796..73558496hg38UCSC Ensembl
Outerchr14:73996500..74025200hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828701
hg1928701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1102n106
Supporting Variantsnssv3980958
SamplesKWS1
Known GenesACOT1, HEATR4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118282
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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