A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978667



Internal ID19242887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:84416353..84447589hg38UCSC Ensembl
Outerchr1:84882036..84913272hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3831237
hg1931237
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116487
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978667
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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