A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509584



Internal ID15825610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:99463978..99536107hg38UCSC Ensembl
Outerchr15:100004183..100076312hg19UCSC Ensembl
Outerchr15:97821706..97893835hg18UCSC Ensembl
Outerchr15:97821706..97893835hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg384083
hg194083
hg184083
hg174083
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv621017
SamplesNA15510
Known Genes
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)nsv509584
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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