A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200380



Internal ID21339195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45434811..45434872hg38UCSC Ensembl
chrX:45294056..45294117hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938206
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200380
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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