A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613657



Internal ID20986728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82969153..82970016hg38UCSC Ensembl
chr7:82598469..82599332hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38864
hg19864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159169
Samples
Known GenesPCLO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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