A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15198102



Internal ID21336898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74369858..74370155hg38UCSC Ensembl
chr7:73784188..73784485hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938823
Supporting Variants
SamplesHG002
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15198102
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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