A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997598



Internal ID16943864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:2909167..2944766hg38UCSC Ensembl
Outerchr7:2948801..2984400hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3835600
hg1935600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950794
Supporting Variants
SamplesBILGI_BIOE
Known GenesCARD11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997598
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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