A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889187



Internal ID22664201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3635481..3641994hg38UCSC Ensembl
chr6:3635715..3642228hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg386514
hg196514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889187
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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