A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3630911



Internal ID11784271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107204752..107204752hg38UCSC Ensembl
chrX:106447982..106447982hg19UCSC Ensembl
chrX:106334638..106334638hg18UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1568973
Supporting Variants
SamplesHuRef
Known GenesNUP62CL
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3630911
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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