A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049005



Internal ID19138224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55014860..55324329hg38UCSC Ensembl
Innerchr10:56774620..57084089hg19UCSC Ensembl
Innerchr10:56444626..56754095hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38309470
hg19309470
hg18309470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519795
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)nsv1049005
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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