A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443952



Internal ID22110133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99827974..99827974hg38UCSC Ensembl
chr10:101587731..101587731hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761603
Samples
Known GenesABCC2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443952
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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