A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586



Internal ID15538314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143718702..143858069hg38UCSC Ensembl
Outerchr7:143415795..143555162hg19UCSC Ensembl
Outerchr7:143046728..143186095hg18UCSC Ensembl
Outerchr7:142853443..142992810hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38139368
hg19139368
hg18139368
hg17139368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7408
Supporting Variants
SamplesNA12878
Known GenesCTAGE6, FAM115A, 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)nssv3586
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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