A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10523



Internal ID15195589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16677941..16769741hg38UCSC Ensembl
Outerchr1:17004436..17096236hg19UCSC Ensembl
Outerchr1:16877023..16968823hg18UCSC Ensembl
Outerchr1:16749742..16841542hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3891801
hg1991801
hg1891801
hg1791801
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18956
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)nssv10523
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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