A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171009



Internal ID21462186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:628593..628846hg38UCSC Ensembl
chrY:539328..539581hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668774
Supporting Variants
SamplesHG02818
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171009
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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