A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008501



Internal ID21917844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131990552..131993794hg38UCSC Ensembl
chr9:134865939..134869181hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594417
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008501
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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