A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200232



Internal ID21339028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85088817..85088866hg38UCSC Ensembl
chrX:84343823..84343872hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951243
Supporting Variants
SamplesHG002
Known GenesAPOOL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200232
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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