A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761708



Internal ID22096205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56397698..56397875hg38UCSC Ensembl
chr16:56431610..56431787hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4448185
Supporting Variants
Samples
Known GenesAMFR
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761708
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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