A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956010



Internal ID17304883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:77241191..77241476hg38UCSC Ensembl
Outerchr7:76870508..76870793hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003734
SamplesBILGI_BIOE
Known GenesCCDC146
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956010
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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