A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017822



Internal ID19107039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116260580..116289519hg38UCSC Ensembl
Innerchr5:115596277..115625216hg19UCSC Ensembl
Innerchr5:115624176..115653115hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3828940
hg1928940
hg1828940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5792n100
Supporting Variantsnssv3647124, nssv3647129, nssv3647127, nssv3647131, nssv3647123, nssv3647122, nssv3647130, nssv3647126, nssv3647125, nssv3647128
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017822
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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