A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142247



Internal ID341447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85786000..85902779hg38UCSC Ensembl
chr7:85415316..85532095hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38116780
hg19116780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142247
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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