A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360556



Internal ID21018109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124861672..124864135hg38UCSC Ensembl
chr3:124580519..124582982hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg382464
hg192464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093402
Samples
Known GenesITGB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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