A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049295



Internal ID18791826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19451367..20220107hg38UCSC Ensembl
Innerchr10:19740296..20509036hg19UCSC Ensembl
Innerchr10:19780302..20549042hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38768741
hg19768741
hg18768741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515834
Samples
Known GenesPLXDC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049295
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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