A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893444



Internal ID22668504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152756644..152763440hg38UCSC Ensembl
chr6:153077779..153084575hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg386797
hg196797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423089
Samples
Known GenesVIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893444
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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