A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951650



Internal ID16953837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152236916..152271215hg38UCSC Ensembl
Outerchr7:151934001..151968300hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3834300
hg1934300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998627
SamplesBILGI_BIOE
Known GenesKMT2C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951650
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer