A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395414



Internal ID21052967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65506303..67062808hg38UCSC Ensembl
chr4:66372021..67928526hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381556506
hg191556506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118305
Samples
Known GenesEPHA5, LOC100144602
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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