A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761659



Internal ID22096162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110456810..110456936hg38UCSC Ensembl
chr13:111109157..111109283hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447549
Supporting Variants
Samples
Known GenesCOL4A2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761659
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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