A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453456



Internal ID22511330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:8806452..8806639hg38UCSC Ensembl
chrY:8674493..8674680hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885382
Supporting Variants
Samples
Known GenesTTTY11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453456
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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