A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315955



Internal ID20849030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232115508..232120371hg38UCSC Ensembl
chr1:232251254..232256117hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg384864
hg194864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058726
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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