A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10890



Internal ID15192792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16680915..16762994hg38UCSC Ensembl
Outerchr1:17007410..17089489hg19UCSC Ensembl
Outerchr1:16879997..16962076hg18UCSC Ensembl
Outerchr1:16752716..16834795hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3882080
hg1982080
hg1882080
hg1782080
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA15510
Known GenesESPNP, LOC729574, MIR3675, MST1L
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)nssv10890
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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