A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8895



Internal ID15534969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:31726789..31771752hg38UCSC Ensembl
Outerchr11:31748337..31793300hg19UCSC Ensembl
Outerchr11:31704913..31749876hg18UCSC Ensembl
Outerchr11:31704913..31749876hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3844964
hg1944964
hg1844964
hg1744964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7727
Supporting Variants
SamplesNA12156
Known GenesELP4
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)nssv8895
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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