A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200695



Internal ID21339491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136999984..137000288hg38UCSC Ensembl
chrX:136082143..136082447hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933921
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200695
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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