A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326708



Internal ID20859845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8987228..9053826hg38UCSC Ensembl
chr1:9047287..9113885hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3866599
hg1966599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064958
Samples
Known GenesSLC2A5, SLC2A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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