A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962789



Internal ID18863322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:18208764..18235006hg38UCSC Ensembl
Outerchr10:18497693..18523935hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3826243
hg1926243
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129353
Supporting Variants
SamplesKWS1
Known GenesCACNB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962789
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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