A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414071



Internal ID21071624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61156537..61166312hg38UCSC Ensembl
chr5:60452364..60462139hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg389776
hg199776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133195
Samples
Known GenesSMIM15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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