A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855361



Internal ID22630296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156789845..156790844hg38UCSC Ensembl
chr7:156582539..156583538hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503399
Samples
Known GenesLMBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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