A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584439



Internal ID21776482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72064898..72065202hg38UCSC Ensembl
chr10:73824656..73824960hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014288
Supporting Variants
Samples
Known GenesSPOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584439
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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