A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634208



Internal ID21582513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2893191..2893191hg38UCSC Ensembl
chr6:2893425..2893425hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142490, nssv17148656, nssv17143246
SamplesHG03732, HG00731, HG03683
Known GenesSERPINB9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634208
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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