A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155242



Internal ID20722282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139100210..139106949hg38UCSC Ensembl
chr7:138784956..138791695hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386740
hg196740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433762
Supporting Variants
Samples
Known GenesZC3HAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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