A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998639



Internal ID16944905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155791807..155809806hg38UCSC Ensembl
Outerchr7:155584501..155602500hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3818000
hg1918000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951662
Supporting Variants
SamplesBILGI_BIOE
Known GenesSHH
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998639
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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