A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404116



Internal ID21061669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161377501..161378400hg38UCSC Ensembl
chr5:160804507..160805406hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126566
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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