A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125358



Internal ID18937135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:73294785..73294866hg38UCSC Ensembl
Outerchr14:73761493..73761574hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983533
SamplesKWS2
Known GenesNUMB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125358
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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