A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499957



Internal ID20873182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1938926..1954671hg38UCSC Ensembl
chr16:1988927..2004672hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3815746
hg1915746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028148
Samples
Known GenesMSRB1, RPL3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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