A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005176



Internal ID7070272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45721205..45721205hg38UCSC Ensembl
chrX:45580442..45580442hg19UCSC Ensembl
chrX:45465386..45465386hg18UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3884
hg1984
hg1884
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3580951
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005176
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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