A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4436934



Internal ID22103111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101509173..101509173hg38UCSC Ensembl
chr8:102521401..102521401hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766114
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4436934
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer