A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326156



Internal ID20859290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91496401..91507100hg38UCSC Ensembl
chr1:91961958..91972657hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203160
Samples
Known GenesCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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