A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953305



Internal ID16955492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63095949..63140848hg38UCSC Ensembl
Outerchr20:61727301..61772200hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3844900
hg1944900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000016
SamplesBILGI_BIOE
Known GenesHAR1A, HAR1B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953305
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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