A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853294



Internal ID22628229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14496935..14499886hg38UCSC Ensembl
chr12:14649869..14652820hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg382952
hg192952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464837
Samples
Known GenesATF7IP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853294
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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