A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10118



Internal ID15542679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:30624637..30659751hg38UCSC Ensembl
Outerchr17:28951655..28986769hg19UCSC Ensembl
Outerchr17:25975781..26010895hg18UCSC Ensembl
Outerchr17:25975781..26010895hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3835115
hg1935115
hg1835115
hg1735115
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7292
Supporting Variants
SamplesNA18956
Known GenesLRRC37BP1, SH3GL1P2
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)nssv10118
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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