A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611467



Internal ID20984538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110927733..111484353hg38UCSC Ensembl
chr6:111248936..111805556hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38556621
hg19556621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216810
Samples
Known GenesGSTM2P1, GTF3C6, KIAA1919, REV3L, RPF2, SLC16A10, TRAF3IP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611467
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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