A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603018



Internal ID20976089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81129501..81137000hg38UCSC Ensembl
chr7:80758817..80766316hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6975n223
Supporting Variantsnssv18160861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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