A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750503



Internal ID21385781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:120347317..120348656hg38UCSC Ensembl
chr2:121104893..121106232hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg381340
hg191340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433555
Supporting Variants
SamplesMDQ010
Known GenesINHBB
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750503
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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