A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200268



Internal ID21339064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141906140..141906245hg38UCSC Ensembl
chrX:140993926..140994031hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928817
Supporting Variants
SamplesHG002
Known GenesMAGEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200268
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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