A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4364442



Internal ID11300294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12614472..12614472hg38UCSC Ensembl
chrY:14726404..14726404hg19UCSC Ensembl
chrY:13235798..13235798hg18UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38628
hg19628
hg18628
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1182657
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4364442
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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