A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6285



Internal ID15190893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81700778..81717870hg38UCSC Ensembl
Outerchr9:84315693..84332785hg19UCSC Ensembl
Outerchr9:83505513..83522605hg18UCSC Ensembl
Outerchr9:81545247..81562339hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3817093
hg1917093
hg1817093
hg1717093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582
Supporting Variants
SamplesNA12156
Known GenesLOC101927502
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)nssv6285
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer