A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1903



Internal ID15194500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16641207..16733522hg38UCSC Ensembl
Outerchr1:16967702..17060017hg19UCSC Ensembl
Outerchr1:16840289..16932604hg18UCSC Ensembl
Outerchr1:16713008..16805323hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3892316
hg1992316
hg1892316
hg1792316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18555
Known GenesESPNP, LOC729574, MIR3675, 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)nssv1903
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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