A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147122



Internal ID346315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29671969..30538747hg38UCSC Ensembl
chr1:30144816..31011594hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38866779
hg19866779
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147122
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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