A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617258



Internal ID20990329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17867901..17869500hg38UCSC Ensembl
chr7:17907524..17909123hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154763
Samples
Known GenesSNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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