A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403530



Internal ID21061083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168693702..168694082hg38UCSC Ensembl
chr5:168120707..168121087hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129539
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403530
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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