A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551652



Internal ID20924783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56491769..56492638hg38UCSC Ensembl
chr20:55066825..55067694hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070416
Samples
Known GenesGCNT7, RTFDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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