A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409016



Internal ID21066569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113054292..113125727hg38UCSC Ensembl
chr5:112389989..112461424hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3871436
hg1971436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123115
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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