A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10882



Internal ID15192784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16633682..16865881hg38UCSC Ensembl
Outerchr1:16960177..17192376hg19UCSC Ensembl
Outerchr1:16832764..17064963hg18UCSC Ensembl
Outerchr1:16705483..16937682hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38232200
hg19232200
hg18232200
hg17232200
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, MST1P2
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)nssv10882
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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