A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818973



Internal ID21264312
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 StatusM
Merged Variants
Supporting Variantsnssv13700730
Samples
Known GenesZFHX4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818973
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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