A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443891



Internal ID21101444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121642905..121643801hg38UCSC Ensembl
chr9:124405184..124406080hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176329
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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