A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952950



Internal ID22728247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34143842..34843201hg38UCSC Ensembl
chr20:32731648..33431004hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38699360
hg19699357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402925
Samples
Known GenesAHCY, ASIP, DYNLRB1, HMGB3P1, ITCH, MAP1LC3A, MIR644A, NCOA6, PIGU, TP53INP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952950
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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