A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446914



Internal ID21104467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121781559..121781845hg38UCSC Ensembl
chr9:124543838..124544124hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176344
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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