A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327965



Internal ID20861109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206887290..206887640hg38UCSC Ensembl
chr1:207060635..207060985hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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