A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7331



Internal ID15205644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:151939875..156013254hg38UCSC Ensembl
Outerchr2:152796389..156869766hg19UCSC Ensembl
Outerchr2:152504635..156578012hg18UCSC Ensembl
Outerchr2:152621897..156695274hg17UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg384073380
hg194073378
hg184073378
hg174073378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1544
SamplesNA19240
Known GenesARL6IP6, CACNB4, FMNL2, GALNT13, KCNJ3, LOC100144595, PRPF40A, RPRM, STAM2
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)nsv7331
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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