A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962781



Internal ID19214937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:103253197..103277630hg38UCSC Ensembl
Outerchr1:103718753..103743186hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3824434
hg1924434
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129346
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962781
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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