A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3692084



Internal ID12069786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16183259..16183259hg38UCSC Ensembl
chrX:16201382..16201382hg19UCSC Ensembl
chrX:16111303..16111303hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38608
hg19608
hg18608
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1336683
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3692084
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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