A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444670



Internal ID22110850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15314602..15314602hg38UCSC Ensembl
chr1:15641098..15641098hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761830
Samples
Known GenesFHAD1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444670
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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