A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147295



Internal ID346477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44576370..44579014hg38UCSC Ensembl
chrX:44435616..44438260hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147295
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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