A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960914



Internal ID19209125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:44710691..44710786hg38UCSC Ensembl
Outerchr6:44678428..44678523hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120155
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960914
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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