A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529066



Internal ID20902427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57373104..57373721hg38UCSC Ensembl
chr19:57884472..57885089hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048602
Samples
Known GenesZNF547
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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