A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603257



Internal ID20976328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82345322..82421064hg38UCSC Ensembl
chr7:81974638..82050380hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3875743
hg1975743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234605
Samples
Known GenesCACNA2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603257
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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