A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377945



Internal ID22435815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75042897..75043235hg38UCSC Ensembl
chr17:73038992..73039330hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931204
Supporting Variants
Samples
Known GenesATP5H
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377945
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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