A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170414



Internal ID21462901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21547372..21547794hg38UCSC Ensembl
chrY:23709258..23709680hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667169
Supporting Variants
SamplesHG03009
Known GenesRBMY1A1, RBMY1B, RBMY1D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170414
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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