A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431157



Internal ID22489027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45053207..45053271hg38UCSC Ensembl
chr7:45092806..45092870hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917370
Supporting Variants
Samples
Known GenesCCM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431157
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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