A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323974



Internal ID20857097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155154037..155167905hg38UCSC Ensembl
chr1:155126513..155140381hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3813869
hg1913869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052061
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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