A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316302



Internal ID20849381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26009718..26021902hg38UCSC Ensembl
chr1:26336209..26348393hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3812185
hg1912185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060565
Samples
Known GenesEXTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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