A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387476



Internal ID21045029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41536372..41546677hg38UCSC Ensembl
chr4:41538389..41548694hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3810306
hg1910306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116361
Samples
Known GenesLIMCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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