A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979025



Internal ID19227862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:43227257..43323687hg38UCSC Ensembl
Outerchr17:41379304..41401055hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3896431
hg1921752
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116524
Supporting Variants
SamplesKWS2
Known GenesLINC00854
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979025
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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