A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750628



Internal ID21384267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3618962..3621492hg38UCSC Ensembl
chr6:3619196..3621726hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382531
hg192531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434964
Supporting Variants
SamplesBTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750628
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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