A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961375



Internal ID19212300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:159397498..159424045hg38UCSC Ensembl
Outerchr3:159115287..159141834hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3826548
hg1926548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110953
Supporting Variants
SamplesKWS1
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961375
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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