A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953306



Internal ID16955493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63151949..63571247hg38UCSC Ensembl
Outerchr20:61783301..62202600hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38419299
hg19419300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000017
SamplesBILGI_BIOE
Known GenesARFGAP1, BIRC7, C20orf195, CHRNA4, COL20A1, EEF1A2, FLJ16779, HELZ2, KCNQ2, MIR124-3, MIR3196, MIR4326, NKAIN4, PPDPF, PTK6, SRMS, YTHDF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953306
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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