A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951652



Internal ID16953839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152281116..152290215hg38UCSC Ensembl
Outerchr7:151978201..151987300hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998629
SamplesBILGI_BIOE
Known GenesKMT2C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951652
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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