A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601195



Internal ID20974266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167949701..168316300hg38UCSC Ensembl
chr6:168350381..168716980hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38366600
hg19366600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6516n223
Supporting Variantsnssv18216053
Samples
Known GenesDACT2, FRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601195
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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