A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076135



Internal ID21985368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159980215..159980215hg38UCSC Ensembl
chr6:160401247..160401247hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571810
Samples
Known GenesIGF2R
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076135
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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