A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569912



Internal ID21518275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136763993..136767960hg38UCSC Ensembl
chr6:137085131..137089098hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg383968
hg193968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154162
SamplesHG03065
Known GenesMAP3K5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569912
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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