A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526901



Internal ID20900262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56488705..56489403hg38UCSC Ensembl
chr19:57000074..57000772hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049329
Samples
Known GenesZNF667-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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