A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688024



Internal ID21209877
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 StatusS
Merged Variantsnsv2799235
Supporting Variants
Samples
Known GenesZNF805
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688024
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.21875


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