A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983554



Internal ID19225949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:24367036..24398775hg38UCSC Ensembl
Outerchr2:24589905..24621644hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3831740
hg1931740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125380
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983554
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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