A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846887



Internal ID22621822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:48162694..48209407hg38UCSC Ensembl
chr7:48202291..48249004hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3846714
hg1946714
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507113
Samples
Known GenesABCA13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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