A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005156



Internal ID16951422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:42277590..42277646hg38UCSC Ensembl
Outerchr1:42743261..42743317hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958710
Supporting Variants
SamplesBILGI_BIOE
Known GenesFOXJ3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005156
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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