A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904361



Internal ID22679538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83333915..83339989hg38UCSC Ensembl
chr6:84043634..84049708hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg386075
hg196075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439043
Samples
Known GenesME1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904361
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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