A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390064



Internal ID22447934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93603909..93611716hg38UCSC Ensembl
chr1:94069466..94077273hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg387808
hg197808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883062
Supporting Variants
Samples
Known GenesBCAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390064
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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