A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441439



Internal ID21098992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88428150..88434026hg38UCSC Ensembl
chr9:91043065..91048941hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg385877
hg195877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187622
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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