A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751118



Internal ID21384194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28900477..28901097hg38UCSC Ensembl
chr1:29226989..29227609hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433110
Supporting Variants
SamplesBTQ016
Known GenesEPB41
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751118
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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