A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517416



Internal ID22575380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7771399..7775864hg38UCSC Ensembl
chrY:7639440..7643905hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg384466
hg194466
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974066
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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