A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7435



Internal ID15205758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123937737..124030780hg38UCSC Ensembl
Outerchr9:126700016..126793059hg19UCSC Ensembl
Outerchr9:125739837..125832880hg18UCSC Ensembl
Outerchr9:123779570..123872613hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3893044
hg1993044
hg1893044
hg1793044
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6296, nssv10682, nssv9474, nssv11204, nssv6297, nssv10683, nssv3749, nssv11205, nssv3750
SamplesNA18517, NA15510, NA18956, NA12156, NA12878
Known GenesLHX2
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)nsv7435
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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