A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330466



Internal ID20863623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42936163..42936706hg38UCSC Ensembl
chr1:43401834..43402377hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060510
Samples
Known GenesSLC2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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