A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100668



Internal ID20667708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45704107..45704699hg38UCSC Ensembl
chr3:45745599..45746191hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360295
Supporting Variants
Samples
Known GenesSACM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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