A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038102



Internal ID18780633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42946153..43147460hg38UCSC Ensembl
Innerchr10:43441601..43642908hg19UCSC Ensembl
Innerchr10:42761607..42962914hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38201308
hg19201308
hg18201308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707779
Samples
Known GenesCSGALNACT2, MIR5100, RET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038102
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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