A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799235



Internal ID21244573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57241575..57241644hg38UCSC Ensembl
chr19:57752943..57753012hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13688024
Samples
Known GenesZNF805
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799235
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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