A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517432



Internal ID22575396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9960213..9963137hg38UCSC Ensembl
chrY:9797822..9800746hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg382925
hg192925
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975896
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517432
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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