A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445010



Internal ID21102563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86288901..86290300hg38UCSC Ensembl
chr9:88903816..88905215hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196159
Samples
Known GenesZCCHC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445010
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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