A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528751



Internal ID20902112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2900838..2971991hg38UCSC Ensembl
chr19:2900836..2971989hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3871154
hg1971154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047434
Samples
Known GenesZNF57, ZNF77
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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