A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1800



Internal ID15194398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:120469875..120479294hg38UCSC Ensembl
Outerchr9:123232153..123241572hg19UCSC Ensembl
Outerchr9:122271974..122281393hg18UCSC Ensembl
Outerchr9:120311707..120321126hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg389420
hg199420
hg189420
hg179420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6699
Supporting Variants
SamplesNA18555
Known GenesCDK5RAP2
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)nssv1800
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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