A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412458



Internal ID21070011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161387601..161389200hg38UCSC Ensembl
chr5:160814607..160816206hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126569
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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