A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799765



Internal ID21245104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2939078..2939182hg38UCSC Ensembl
chr19:2939076..2939180hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677506
Samples
Known GenesZNF77
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799765
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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