A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444194



Internal ID22110374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95986203..95986203hg38UCSC Ensembl
chr10:97745960..97745960hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757599
Samples
Known GenesENTPD1-AS1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444194
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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