A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262231



Internal ID20471449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:785200..785277hg38UCSC Ensembl
chr7:824837..824914hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730923
Supporting Variants
Samples
Known GenesHEATR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262231
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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