A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330236



Internal ID20863392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174005486..174009027hg38UCSC Ensembl
chr1:173974624..173978165hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg383542
hg193542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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