A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454156



Internal ID21111709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127181437..127187366hg38UCSC Ensembl
chr9:129943716..129949645hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385930
hg195930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176791
Samples
Known GenesRALGPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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