A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410348



Internal ID21067901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113304924..113321819hg38UCSC Ensembl
chr5:112640621..112657516hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3816896
hg1916896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123137
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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