A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142200



Internal ID341400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4679263..4681994hg38UCSC Ensembl
chr10:4721455..4724186hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382732
hg192732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142200
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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