A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979994



Internal ID54047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7805999..7835061hg38UCSC Ensembl
chr6:7806232..7835294hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3829063
hg1929063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472362
Supporting Variants
Samples
Known GenesBMP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979994
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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