A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509076



Internal ID15476574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:95201395..95216953hg38UCSC Ensembl
Outerchr5:94537099..94552657hg19UCSC Ensembl
Outerchr5:94562855..94578413hg18UCSC Ensembl
Outerchr5:94562855..94578413hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3816400
hg1916400
hg1816400
hg1716400
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv623449, nssv619419
SamplesNA18994, NA10860
Known GenesMCTP1
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nsv509076
Frequency
Sample Size4
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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