A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142494



Internal ID341694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:767766..768292hg38UCSC Ensembl
chr7:807403..807929hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991423
Samples
Known GenesHEATR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142494
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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