A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334156



Internal ID20867338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151074597..151078950hg38UCSC Ensembl
chr1:151047073..151051426hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg384354
hg194354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053017
Samples
Known GenesGABPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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