A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444625



Internal ID21102178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127575245..127587003hg38UCSC Ensembl
chr9:130337524..130349282hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3811759
hg1911759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176810
Samples
Known GenesFAM129B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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