A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530018



Internal ID20903379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35707601..35709200hg38UCSC Ensembl
chr20:34295523..34297122hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068012
Samples
Known GenesRBM39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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