A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038023



Internal ID18780554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6965209..7161146hg38UCSC Ensembl
Innerchr10:7007171..7203108hg19UCSC Ensembl
Innerchr10:7047177..7243114hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38195938
hg19195938
hg18195938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3485271
Samples
Known GenesSFMBT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038023
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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