A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043245



Internal ID18785776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70290210..70915897hg38UCSC Ensembl
Innerchr10:72049966..72675654hg19UCSC Ensembl
Innerchr10:71719972..72345660hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38625688
hg19625689
hg18625689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516032
Samples
Known GenesADAMTS14, EIF4EBP2, LRRC20, NODAL, PALD1, PCBD1, PRF1, SGPL1, TBATA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043245
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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