A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418325



Internal ID21075878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31604948..31644080hg38UCSC Ensembl
chr9:31604946..31644078hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3839133
hg1939133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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