A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142442



Internal ID341642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35108027..35380842hg38UCSC Ensembl
chr10:35396955..35669770hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38272816
hg19272816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031525
Samples
Known GenesCCNY, CREM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142442
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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