A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767185



Internal ID22101656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21057589..21057589hg38UCSC Ensembl
chr10:21346518..21346518hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4449000
Supporting Variants
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767185
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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