A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762056



Internal ID22096553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6355671..6355797hg38UCSC Ensembl
chr19:6355682..6355808hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeOTHER delins
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4439770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762056
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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