A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452448



Internal ID21110001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137413376..137443504hg38UCSC Ensembl
chr9:140307828..140337956hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3830129
hg1930129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176416
Samples
Known GenesENTPD8, EXD3, NOXA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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