A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396314



Internal ID21053867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113331101..113337800hg38UCSC Ensembl
chr5:112666798..112673497hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123139
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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