A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004772



Internal ID17297724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:7502670..7502999hg38UCSC Ensembl
Outerchr7:7542301..7542630hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958399
Supporting Variants
SamplesBILGI_BIOE
Known GenesCOL28A1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004772
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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