A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609953



Internal ID21558258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34541466..34541466hg38UCSC Ensembl
chr1:35007067..35007067hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065291
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609953
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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