A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739197



Internal ID20515170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70782999..70783063hg38UCSC Ensembl
chr6:71492702..71492766hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270250
Samples
Known GenesSMAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739197
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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