A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441271



Internal ID21098824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125071601..125074600hg38UCSC Ensembl
chr9:127833880..127836879hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176650
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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