A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605781



Internal ID20978852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167346901..167555300hg38UCSC Ensembl
chr6:167760389..167942073hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38208400
hg19181685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217049
Samples
Known GenesTCP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605781
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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