A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430961



Internal ID22488831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129201247..129201880hg38UCSC Ensembl
chr7:128841088..128841721hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923593
Supporting Variants
Samples
Known GenesSMO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430961
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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