A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627556



Internal ID21575861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136970330..136970330hg38UCSC Ensembl
chr6:137291468..137291468hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148090
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627556
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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