A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607437



Internal ID21555742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3141033..3141033hg38UCSC Ensembl
chrY:3009074..3009074hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170119
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607437
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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