A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106550



Internal ID21451096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7910782..7910871hg38UCSC Ensembl
chr19:7975667..7975756hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588670
Supporting Variants
SamplesHG01505
Known GenesMAP2K7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106550
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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