A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315629



Internal ID20848700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197172978..197173383hg38UCSC Ensembl
chr1:197142108..197142513hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056392
Samples
Known GenesZBTB41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315629
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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