A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869238



Internal ID22644173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7111621..7117708hg38UCSC Ensembl
chr17:7014940..7021027hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386088
hg196088
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475876
Samples
Known GenesASGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869238
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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