A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327809



Internal ID20860951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207208210..207222660hg38UCSC Ensembl
chr1:207381555..207396005hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3814451
hg1914451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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