A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436505



Internal ID21094058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100020755..100021573hg38UCSC Ensembl
chr9:102783037..102783855hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171520
Samples
Known GenesERP44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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