A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993522



Internal ID19242109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:41408445..41408505hg38UCSC Ensembl
Outerchr6:41376183..41376243hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142010
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993522
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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