A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155222



Internal ID20722262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138622571..138685142hg38UCSC Ensembl
chr7:138307316..138369887hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3862572
hg1962572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424954
Supporting Variants
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155222
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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