A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748508



Internal ID21386265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139134871..139136267hg38UCSC Ensembl
chr6:139456008..139457404hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381397
hg191397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434765
Supporting Variants
SamplesMDQ010
Known GenesHECA
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748508
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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