A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747152



Internal ID21387281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139424928..139425330hg38UCSC Ensembl
chr7:139109674..139110076hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435102
Supporting Variants
SamplesMDQ045
Known GenesLOC100129148
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747152
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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