A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332941



Internal ID20866116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156269599..156270819hg38UCSC Ensembl
chr1:156239390..156240610hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052259
Samples
Known GenesSMG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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