A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962815



Internal ID18862069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:60108768..60137807hg38UCSC Ensembl
Outerchr14:60575486..60604525hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3829040
hg1929040
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129376
Supporting Variants
SamplesKWS1
Known GenesPCNXL4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962815
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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