A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668723



Internal ID21617028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2631035..2631091hg38UCSC Ensembl
chrY:2499076..2499132hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170477
SamplesHG03732
Known GenesCD99P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668723
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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