A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944632



Internal ID22720100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56622034..56622117hg38UCSC Ensembl
chr19:57133402..57133485hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395832
Samples
Known GenesZNF71
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944632
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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