A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846930



Internal ID22621865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32579743..32583178hg38UCSC Ensembl
chr7:32619355..32622790hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg383436
hg193436
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505511
Samples
Known GenesAVL9, DPY19L1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846930
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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