A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983469



Internal ID19226770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:29454362..30375065hg38UCSC Ensembl
Outerchr1:29780874..30847912hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38920704
hg191067039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125297
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983469
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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