A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476452



Internal ID22534350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76516278..76518407hg38UCSC Ensembl
chr17:74512360..74514489hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382130
hg192130
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476452
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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