A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970694



Internal ID22745629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2934285..2936711hg38UCSC Ensembl
chrY:2802326..2804752hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg382427
hg192427
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517366
Samples
Known GenesZFY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970694
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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