A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181523



Internal ID21320319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70918724..70918879hg38UCSC Ensembl
chr10:72678481..72678636hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938858
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181523
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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