A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029002



Internal ID87034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6590207..6590207hg38UCSC Ensembl
chr10:6632169..6632169hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029002
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.03044


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