A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327907



Internal ID20861051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:230593383..230609219hg38UCSC Ensembl
chr1:230729129..230744965hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3815837
hg1915837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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