A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368854



Internal ID22594523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7207479..7207529hg38UCSC Ensembl
chr10:7249441..7249491hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908573
Supporting Variants
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368854
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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