A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569873



Internal ID21518235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151499013..151499356hg38UCSC Ensembl
chr6:151820148..151820491hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143012
SamplesHG00732
Known GenesCCDC170
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569873
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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