A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961337



Internal ID19206546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:13115618..13141826hg38UCSC Ensembl
Outerchr17:13018935..13045143hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3826209
hg1926209
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110919
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961337
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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