A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700730



Internal ID21222569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76644959..76645126hg38UCSC Ensembl
chr8:77557194..77557361hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818973
Supporting Variants
Samples
Known GenesZFHX4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700730
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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