A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895968



Internal ID6302979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103885557..103987875hg19UCSC Ensembl
Outerchr10:103772270..104004195hg19UCSC Ensembl
Innerchr10:103875547..103977865hg18UCSC Ensembl
Outerchr10:103762260..103994185hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1546745
SamplesMS17208
Known GenesC10orf76, ELOVL3, HPS6, LDB1, NOLC1, PITX3, PPRC1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895968
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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