A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3750



Internal ID15191792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123978320..124030780hg38UCSC Ensembl
Outerchr9:126740599..126793059hg19UCSC Ensembl
Outerchr9:125780420..125832880hg18UCSC Ensembl
Outerchr9:123820153..123872613hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3852461
hg1952461
hg1852461
hg1752461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7435
Supporting Variants
SamplesNA12878
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)nssv3750
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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