A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333032



Internal ID20866207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93678205..93683383hg38UCSC Ensembl
chr1:94143761..94148939hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg385179
hg195179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065580
Samples
Known GenesBCAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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