A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751714



Internal ID21384386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111597733..111599066hg38UCSC Ensembl
chr6:111918936..111920269hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434727
Supporting Variants
SamplesBTQ016
Known GenesTRAF3IP2, TRAF3IP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751714
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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