A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400251



Internal ID21057804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94671401..94672200hg38UCSC Ensembl
chr5:94007106..94007905hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136472
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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