A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377385



Internal ID21034938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105690321..105690770hg38UCSC Ensembl
chr4:106611478..106611927hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107004
Samples
Known GenesINTS12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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