A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414737



Internal ID21072290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133008304..133017876hg38UCSC Ensembl
chr5:132343996..132353568hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg389573
hg199573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127157
Samples
Known GenesZCCHC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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