A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444917



Internal ID21102470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130433997..130437981hg38UCSC Ensembl
chr9:133309384..133313368hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383985
hg193985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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