A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951651



Internal ID16953838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152273616..152280515hg38UCSC Ensembl
Outerchr7:151970701..151977600hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998628
SamplesBILGI_BIOE
Known GenesKMT2C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951651
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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