A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616014



Internal ID21564319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2632009..2632009hg38UCSC Ensembl
chrY:2500050..2500050hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170478
SamplesNA19239
Known GenesCD99P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616014
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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