A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453077



Internal ID21110630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91631901..91641000hg38UCSC Ensembl
chr9:94394183..94403282hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187375
Samples
Known GenesMIR3910-1, MIR3910-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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