A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509435



Internal ID22567385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93546991..93593008hg38UCSC Ensembl
chr7:93176303..93222320hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3846018
hg1946018
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850448
Supporting Variants
Samples
Known GenesCALCR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509435
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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