A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440607



Internal ID21098160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103918832..103945867hg38UCSC Ensembl
chr9:106681113..106708148hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3827036
hg1927036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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