A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573560



Internal ID21765603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107654907..107654994hg38UCSC Ensembl
chr6:107976111..107976198hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012240
Supporting Variants
Samples
Known GenesSOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573560
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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