A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950977



Internal ID16953164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:74164943..74171842hg38UCSC Ensembl
Outerchr10:75924701..75931600hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998009
SamplesBILGI_BIOE
Known GenesADK
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950977
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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