A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446617



Internal ID22112795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96712355..96712527hg38UCSC Ensembl
chr6:97160231..97160403hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766463
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446617
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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