A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438944



Internal ID22105121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1051543..1051543hg38UCSC Ensembl
chr6:1051778..1051778hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767498
Samples
Known GenesLOC285768
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438944
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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