A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961272



Internal ID18863333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:47894964..48516423hg38UCSC Ensembl
Outerchr20:46523708..47132961hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38621460
hg19609254
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110861
Supporting Variants
SamplesKWS1
Known GenesLINC00494
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961272
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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