A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155255



Internal ID20722295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139424856..139425206hg38UCSC Ensembl
chr7:139109602..139109952hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424751
Supporting Variants
Samples
Known GenesLOC100129148
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.34037


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