A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954588



Internal ID21374657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13118908..13120450hg38UCSC Ensembl
chrY:15230822..15232364hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381543
hg191543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200449
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954588
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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