A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449957



Internal ID21107510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36134675..36148130hg38UCSC Ensembl
chr9:36134672..36148127hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3813456
hg1913456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185813
Samples
Known GenesGLIPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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