A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409253



Internal ID21066806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82286277..82315182hg38UCSC Ensembl
chr5:81582096..81611001hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3828906
hg1928906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132969
Samples
Known GenesATP6AP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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