A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322980



Internal ID20856095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17671228..17677360hg38UCSC Ensembl
chr1:17997723..18003855hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg386133
hg196133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053754
Samples
Known GenesARHGEF10L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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