A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978678



Internal ID19243048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:80737144..80737235hg38UCSC Ensembl
Outerchr10:82496900..82496991hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116496
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978678
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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