A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453079



Internal ID21110632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31003363..31003733hg38UCSC Ensembl
chr10:31292292..31292662hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981428
Samples
Known GenesZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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