A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413714



Internal ID21071267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73029776..73030264hg38UCSC Ensembl
chr5:72325603..72326091hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132182
Samples
Known GenesFCHO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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