A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296328



Internal ID20505546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126982012..126982133hg38UCSC Ensembl
chr7:126622066..126622187hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741573
Supporting Variants
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296328
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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