A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410461



Internal ID21068014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52874801..52875700hg38UCSC Ensembl
chr5:52170635..52171534hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132320
Samples
Known GenesITGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410461
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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