A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398448



Internal ID21056001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123070715..123136079hg38UCSC Ensembl
chr5:122406410..122471774hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3865365
hg1965365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123864
Samples
Known GenesPRDM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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