A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853499



Internal ID22628434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100121106..100134130hg38UCSC Ensembl
chr7:99718729..99731753hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3813025
hg1913025
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503217
Samples
Known GenesCNPY4, MBLAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853499
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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