A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9405



Internal ID15193670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16674307..16773011hg38UCSC Ensembl
Outerchr1:17000802..17099506hg19UCSC Ensembl
Outerchr1:16873389..16972093hg18UCSC Ensembl
Outerchr1:16746108..16844812hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3898705
hg1998705
hg1898705
hg1798705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18517
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)nssv9405
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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