A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440183



Internal ID21097736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121613565..121651792hg38UCSC Ensembl
chr9:124375844..124414071hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3838228
hg1938228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176323
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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