A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997141



Internal ID16943407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:44607229..44652328hg38UCSC Ensembl
Outerchr1:45072901..45118000hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3845100
hg1945100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950704
Supporting Variants
SamplesBILGI_BIOE
Known GenesRNF220
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997141
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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