A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997956



Internal ID16944222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:43137753..43161752hg38UCSC Ensembl
Outerchr10:43633201..43657200hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3824000
hg1924000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951565
Supporting Variants
SamplesBILGI_BIOE
Known GenesCSGALNACT2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997956
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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