A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324072



Internal ID20857196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75367216..75367983hg38UCSC Ensembl
chr1:75832901..75833668hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064026
Samples
Known GenesSLC44A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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