A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6533



Internal ID15190645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2512559..2553994hg38UCSC Ensembl
Outerchr1:2443998..2485433hg19UCSC Ensembl
Outerchr1:2433858..2488860hg18UCSC Ensembl
Outerchr1:2476160..2531162hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3841436
hg1941436
hg1855003
hg1755003
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7171
Supporting Variants
SamplesNA12156
Known GenesHES5, LOC100133445, LOC115110, PANK4, TNFRSF14
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)nssv6533
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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