A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157283



Internal ID21472410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160601521..160603270hg38UCSC Ensembl
chr6:161022553..161024302hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566057
Supporting Variants
SamplesHG03125
Known GenesLPA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157283
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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