A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767522



Internal ID22101999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143012537..143012537hg38UCSC Ensembl
chr5:142392102..142392102hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4449485
Supporting Variants
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767522
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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