A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618171



Internal ID20991242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84150519..84152678hg38UCSC Ensembl
chr7:83779835..83781994hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382160
hg192160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161697
Samples
Known GenesSEMA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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