A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855352



Internal ID22630287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129445715..129446714hg38UCSC Ensembl
chr7:129085556..129086555hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501226, nssv17501225
Samples
Known GenesSTRIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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