A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611662



Internal ID20984733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82171131..82873362hg38UCSC Ensembl
chr7:81800447..82502678hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38702232
hg19702232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6977n223
Supporting Variantsnssv18234490
Samples
Known GenesCACNA2D1, PCLO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611662
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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