A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200638



Internal ID21339445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26194092..26194218hg38UCSC Ensembl
chrX:26212209..26212335hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3947932
Supporting Variants
SamplesHG002
Known GenesMAGEB6
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200638
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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