A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137922



Internal ID337103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144792355..144889911hg38UCSC Ensembl
chrX:143873876..143971431hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3897557
hg1997556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137922
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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