A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200294



Internal ID21339090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148547139..148547216hg38UCSC Ensembl
chrX:147628660..147628737hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3932224
Supporting Variants
SamplesHG002
Known GenesAFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200294
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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