A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962862



Internal ID19207142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:108652916..108652996hg38UCSC Ensembl
Outerchr4:109574072..109574152hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129420
Supporting Variants
SamplesKWS1
Known GenesOSTC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962862
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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