A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923670



Internal ID22698897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156505882..156521130hg38UCSC Ensembl
chr7:156298576..156313824hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3815249
hg1915249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449310
Samples
Known GenesLINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923670
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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