A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10774



Internal ID15542024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26599082..26647485hg38UCSC Ensembl
Outerchr1:26925573..26973976hg19UCSC Ensembl
Outerchr1:26798160..26846563hg18UCSC Ensembl
Outerchr1:26609715..26658118hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3848404
hg1948404
hg1848404
hg1748404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7175
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10774
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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