A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438441



Internal ID22104621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41633302..41633519hg38UCSC Ensembl
chr17:39789554..39789771hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765391
Samples
Known GenesKRT42P
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SUBSINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438441
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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