A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412065



Internal ID21069618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120616238..120616824hg38UCSC Ensembl
chr5:119951933..119952519hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124707
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412065
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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