A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437199



Internal ID21094752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127195046..127199357hg38UCSC Ensembl
chr9:129957325..129961636hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384312
hg194312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176793
Samples
Known GenesRALGPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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