A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952989



Internal ID17301863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:15615056..15620955hg38UCSC Ensembl
Outerchr20:15595701..15601600hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999925
SamplesBILGI_BIOE
Known GenesMACROD2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952989
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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