A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997095



Internal ID17290047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:23958011..23970110hg38UCSC Ensembl
Outerchr1:24284501..24296600hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950285
Supporting Variants
SamplesBILGI_BIOE
Known GenesPNRC2, SRSF10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997095
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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