A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11156



Internal ID15192737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101000302..101018906hg38UCSC Ensembl
Outerchr7:100643583..100662187hg19UCSC Ensembl
Outerchr7:100430303..100448907hg18UCSC Ensembl
Outerchr7:100237018..100255622hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3816166
hg1916166
hg1816166
hg1716166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5872
Supporting Variants
SamplesNA15510
Known GenesMUC12
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)nssv11156
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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