A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037805



Internal ID19127024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123752404..123788948hg38UCSC Ensembl
Innerchr10:125511920..125548464hg19UCSC Ensembl
Innerchr10:125501910..125538454hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3836545
hg1936545
hg1836545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv988n100
Supporting Variantsnssv3511449, nssv3505267
Samples
Known GenesCPXM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037805
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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