A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202830



Internal ID21341631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73205683..73205683hg38UCSC Ensembl
chr6:73915406..73915406hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954379
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202830
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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