A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3885



Internal ID15191926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16679982..16766118hg38UCSC Ensembl
Outerchr1:17006477..17092613hg19UCSC Ensembl
Outerchr1:16879064..16965200hg18UCSC Ensembl
Outerchr1:16751783..16837919hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3886137
hg1986137
hg1886137
hg1786137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA12878
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)nssv3885
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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