A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9654



Internal ID15540149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:187918185..187953428hg38UCSC Ensembl
Outerchr4:188839339..188874582hg19UCSC Ensembl
Outerchr4:189076333..189111576hg18UCSC Ensembl
Outerchr4:189214488..189249731hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3835244
hg1935244
hg1835244
hg1735244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7367
Supporting Variants
SamplesNA18507
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9654
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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