A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9730



Internal ID15539943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143726899..143846255hg38UCSC Ensembl
Outerchr7:143423992..143543348hg19UCSC Ensembl
Outerchr7:143054925..143174281hg18UCSC Ensembl
Outerchr7:142861640..142980996hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38119357
hg19119357
hg18119357
hg17119357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7408
Supporting Variants
SamplesNA18507
Known GenesCTAGE6, FAM115C, LOC154761
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)nssv9730
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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