A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323831



Internal ID20856953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182150547..182152101hg38UCSC Ensembl
chr1:182119682..182121236hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381555
hg191555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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