A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857300



Internal ID22632235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72924972..72926320hg38UCSC Ensembl
chr7:72395510..72396858hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381349
hg191349
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509289, nssv17502740
Samples
Known GenesPOM121
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857300
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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