A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038398



Internal ID18780929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7501987..7614812hg38UCSC Ensembl
Innerchr10:7543949..7656775hg19UCSC Ensembl
Innerchr10:7583955..7696781hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38112826
hg19112827
hg18112827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707683
Samples
Known GenesITIH5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038398
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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