A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873038



Internal ID22647981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2990176..2990227hg38UCSC Ensembl
chrY:2858217..2858268hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873038
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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