A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987905



Internal ID19216258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:75693099..75693206hg38UCSC Ensembl
Outerchr5:74988924..74989031hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133093
Supporting Variants
SamplesKWS1
Known GenesPOC5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987905
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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