A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156234



Internal ID21482070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71561359..71563555hg38UCSC Ensembl
chr6:72271062..72273258hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382197
hg192197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577179
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156234
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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