A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868808



Internal ID22643743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38342041..38346719hg38UCSC Ensembl
chr17:36497924..36502601hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384679
hg194678
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473725
Samples
Known GenesGPR179
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868808
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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