A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200433



Internal ID21339229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152007277..152007469hg38UCSC Ensembl
chrX:151175749..151175941hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953183
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200433
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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