A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038386



Internal ID18780917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2139891..2308700hg38UCSC Ensembl
Innerchr10:2182085..2350894hg19UCSC Ensembl
Innerchr10:2172085..2340894hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38168810
hg19168810
hg18168810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3498717
Samples
Known GenesLINC00701
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038386
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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