A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170683



Internal ID21501156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:326254..326813hg38UCSC Ensembl
chrY:236989..237548hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671841
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170683
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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