A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6461



Internal ID15190717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:60487120..60519417hg38UCSC Ensembl
Outerchr11:60254593..60286890hg19UCSC Ensembl
Outerchr11:60011169..60043466hg18UCSC Ensembl
Outerchr11:60011169..60043466hg17UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg387130
hg197130
hg187130
hg177130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv337
Supporting Variants
SamplesNA12156
Known GenesMS4A12, MS4A13
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)nssv6461
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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