A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038131



Internal ID18780662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7416409..7706490hg38UCSC Ensembl
Innerchr10:7458371..7748453hg19UCSC Ensembl
Innerchr10:7498377..7788459hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38290082
hg19290083
hg18290083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3485697
Samples
Known GenesITIH2, ITIH5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038131
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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