A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444654



Internal ID22110834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136429..35137030hg38UCSC Ensembl
chr6:35104206..35104807hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764172
Samples
Known GenesTCP11
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444654
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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