A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506673



Internal ID22564621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43149488..43173732hg38UCSC Ensembl
chr8:43004631..43028875hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3824245
hg1924245
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849062
Supporting Variants
Samples
Known GenesHGSNAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506673
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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