A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433651



Internal ID22491521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52736060..52743496hg38UCSC Ensembl
chr6:52600858..52608294hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg387437
hg197437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895193
Supporting Variants
Samples
Known GenesGSTA7P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433651
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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