A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287140



Internal ID20496358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151498957..151499344hg38UCSC Ensembl
chr6:151820092..151820479hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746132
Supporting Variants
Samples
Known GenesCCDC170
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287140
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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