A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1587828



Internal ID12750949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12513525..12513525hg38UCSC Ensembl
chrY:14625257..14625257hg19UCSC Ensembl
chrY:13135265..13135265hg18UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3868
hg1968
hg1868
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3661182
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1587828
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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