A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3763390



Internal ID11998480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:99903900..99903952hg38UCSC Ensembl
chrX:99158898..99158950hg19UCSC Ensembl
chrX:99045554..99045606hg18UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1335652
Supporting Variants
SamplesHuRef
Known GenesXRCC6P5
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3763390
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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