A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv813n71



Internal ID6318433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102749069..102775205hg19UCSC Ensembl
chr10:102739059..102765195hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv895965, nsv895962
SamplesSP54956, SP54043
Known GenesC10orf2, LZTS2, PDZD7
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv813n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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