A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378152



Internal ID21035705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76567528..76579292hg38UCSC Ensembl
chr4:77488681..77500445hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3811765
hg1911765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120273
Samples
Known GenesMIR4450, SHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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