A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948978



Internal ID21369047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7720499..7720499hg38UCSC Ensembl
chrY:7588540..7588540hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg383326
hg193326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205798
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948978
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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