A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5471779



Internal ID249508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7560402..7560540hg38UCSC Ensembl
chr6:7560635..7560773hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979981
Samples
Known GenesDSP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5471779
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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