A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9449



Internal ID15540400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143727783..143845977hg38UCSC Ensembl
Outerchr7:143424876..143543070hg19UCSC Ensembl
Outerchr7:143055809..143174003hg18UCSC Ensembl
Outerchr7:142862524..142980718hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38118195
hg19118195
hg18118195
hg17118195
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7408
Supporting Variants
SamplesNA18517
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)nssv9449
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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