A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1924



Internal ID15194521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3281469..3362675hg38UCSC Ensembl
Outerchr11:3302699..3383905hg19UCSC Ensembl
Outerchr11:3259275..3340481hg18UCSC Ensembl
Outerchr11:3259275..3340481hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3881207
hg1981207
hg1881207
hg1781207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7649
Supporting Variants
SamplesNA18555
Known GenesZNF195
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)nssv1924
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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