A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765938



Internal ID22100409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140233596..140233596hg38UCSC Ensembl
chr7:139933396..139933396hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447133
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765938
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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