A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415563



Internal ID21073116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113196727..113284716hg38UCSC Ensembl
chr5:112532424..112620413hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3887990
hg1987990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123126
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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