A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141707



Internal ID21419697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98140130..98140196hg38UCSC Ensembl
chr7:97769442..97769508hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567830
Supporting Variants
SamplesHG00731
Known GenesLMTK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141707
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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