A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437814



Internal ID22495684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120960390..120960540hg38UCSC Ensembl
chr7:120600444..120600594hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912833
Supporting Variants
Samples
Known GenesING3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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