A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327595



Internal ID20860735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12715500..12716123hg38UCSC Ensembl
chr1:12775503..12776126hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051419
Samples
Known GenesAADACL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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