A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330654



Internal ID20863812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177364103..177380255hg38UCSC Ensembl
chr1:177333239..177349391hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3816153
hg1916153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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