A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385406



Internal ID21042959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12507045..12870976hg38UCSC Ensembl
chr5:12507157..12871088hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38363932
hg19363932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124580
Samples
Known GenesCT49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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