A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3973827



Internal ID11788046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18992642..18992642hg38UCSC Ensembl
chrY:21154528..21154528hg19UCSC Ensembl
chrY:19613916..19613916hg18UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg382741
hg192741
hg182741
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1565023
Supporting Variants
SamplesHuRef
Known GenesCD24, TTTY14
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3973827
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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