A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873209



Internal ID22648153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12088125..12088190hg38UCSC Ensembl
chrY:14208831..14208896hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873209
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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