A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334835



Internal ID20868024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157886710..157887571hg38UCSC Ensembl
chr1:157856500..157857361hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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