A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766742



Internal ID22101216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206524558..206524558hg38UCSC Ensembl
chr1:206697891..206697891hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4438158
Supporting Variants
Samples
Known GenesRASSF5
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766742
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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