A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534077



Internal ID20907438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44007468..44008131hg38UCSC Ensembl
chr19:44511620..44512283hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048139
Samples
Known GenesZNF230
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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