A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993365



Internal ID19238535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:118771427..118773043hg38UCSC Ensembl
Outerchr2:119529003..119530619hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg381617
hg191617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141859
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993365
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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