A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15763265



Internal ID22097718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119096338..119096666hg38UCSC Ensembl
chr6:119417503..119417831hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445917
Supporting Variants
Samples
Known GenesFAM184A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15763265
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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