A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316931



Internal ID20850013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157017574..157019902hg38UCSC Ensembl
chr1:156987366..156989694hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382329
hg192329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052294
Samples
Known GenesARHGEF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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