A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862502



Internal ID22637437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31716000..31716999hg38UCSC Ensembl
chr12:31868934..31869933hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463617
Samples
Known GenesAMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862502
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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