A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670195



Internal ID21618502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6241395..6241764hg38UCSC Ensembl
chrY:6109436..6109805hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170783
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670195
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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