A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049521



Internal ID19138740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89183210..89197932hg38UCSC Ensembl
Innerchr10:90942967..90957689hg19UCSC Ensembl
Innerchr10:90932947..90947669hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3814723
hg1914723
hg1814723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv950n100
Supporting Variantsnssv3514125, nssv3516507, nssv3505805, nssv3522642
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)nsv1049521
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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