A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997068



Internal ID16943334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1062161..1071260hg38UCSC Ensembl
Outerchr10:1108101..1117200hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951232
Supporting Variants
SamplesBILGI_BIOE
Known GenesWDR37
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997068
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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