A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116557



Internal ID18938271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:115953455..115985933hg38UCSC Ensembl
Outerchr6:116274618..116307096hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3832479
hg1932479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961397, nssv3993528
SamplesKWS2, KWS1
Known GenesFRK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116557
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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