A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144892



Internal ID344097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55505825..55506195hg38UCSC Ensembl
chr16:55539737..55540107hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705976
Samples
Known GenesMMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144892
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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