A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857152



Internal ID22632087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156505877..156517464hg38UCSC Ensembl
chr7:156298571..156310158hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3811588
hg1911588
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504647
Samples
Known GenesLINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857152
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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