A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582905



Internal ID21531422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2888823..2889236hg38UCSC Ensembl
chr6:2889057..2889470hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146356
SamplesHG02587
Known GenesSERPINB9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582905
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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