A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613100



Internal ID21561405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1401088..1401088hg38UCSC Ensembl
chrY:1469981..1469981hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169467
SamplesHG02818
Known GenesASMTL-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613100
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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