A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978499



Internal ID22753434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:16100684..16102583hg38UCSC Ensembl
chrY:18212564..18214463hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978499
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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