A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433774



Internal ID22491644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143386082..143386427hg38UCSC Ensembl
chr7:143083175..143083520hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924213
Supporting Variants
Samples
Known GenesZYX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433774
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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