A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610345



Internal ID20983416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121271285..121298314hg38UCSC Ensembl
chr7:120911339..120938368hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3827030
hg1927030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218128
Samples
Known GenesCPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610345
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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