A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200253



Internal ID21339049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121199097..121199155hg38UCSC Ensembl
chrX:120332951..120333009hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954040
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200253
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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