A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517065



Internal ID22575028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14020998..14119394hg38UCSC Ensembl
chrY:16132878..16231274hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3898397
hg1998397
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972021
Supporting Variants
Samples
Known GenesVCY, VCY1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517065
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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