A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270830



Internal ID20480048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107770163..107770257hg38UCSC Ensembl
chr7:107410608..107410702hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738385
Supporting Variants
Samples
Known GenesSLC26A3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270830
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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