A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004875



Internal ID17297827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:118197943..118198061hg38UCSC Ensembl
Outerchr10:119957455..119957573hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958495
Supporting Variants
SamplesBILGI_BIOE
Known GenesCASC2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004875
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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