A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327548



Internal ID20860688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203965401..203976200hg38UCSC Ensembl
chr1:203934529..203945328hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3810800
hg1910800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327548
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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