A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038525



Internal ID19127744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55679434..55968157hg38UCSC Ensembl
Innerchr10:57439194..57727917hg19UCSC Ensembl
Innerchr10:57109200..57397923hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38288724
hg19288724
hg18288724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv867n100
Supporting Variantsnssv3516703, nssv3514498, nssv3505314, nssv3505464, nssv3522466, nssv3508819, nssv3507841, nssv3506681, nssv3519922
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038525
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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