A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263756



Internal ID20472974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87736822..87736884hg38UCSC Ensembl
chr6:88446540..88446602hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743862
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263756
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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