A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951360



Internal ID16953547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:76476184..76541183hg38UCSC Ensembl
Outerchr7:76105501..76170500hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3865000
hg1965000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998529
SamplesBILGI_BIOE
Known GenesDTX2, UPK3B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951360
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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