A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609832



Internal ID21558137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66608987..66608987hg38UCSC Ensembl
chr1:67074670..67074670hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066384
SamplesHG03371
Known GenesSGIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609832
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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