A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972021



Internal ID22746956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14020998..14119394hg38UCSC Ensembl
chrY:16132878..16231274hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3898397
hg1998397
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517065, nssv17517066
Samples
Known GenesVCY, VCY1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972021
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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