A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4208997



Internal ID11144849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17484633..17484702hg38UCSC Ensembl
chrX:17502756..17502825hg19UCSC Ensembl
chrX:17412677..17412746hg18UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3870
hg1970
hg1870
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1495197
Supporting Variants
SamplesHuRef
Known GenesNHS
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4208997
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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