A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202002



Internal ID21340808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81639560..81639560hg38UCSC Ensembl
chr6:82349277..82349277hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925149
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202002
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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