A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997198



Internal ID16943464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:111980679..111990978hg38UCSC Ensembl
Outerchr1:112523301..112533600hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951394
Supporting Variants
SamplesBILGI_BIOE
Known GenesKCND3, LOC643355
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997198
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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