A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003141



Internal ID16949407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16961106..17013905hg38UCSC Ensembl
Outerchr1:17287601..17340400hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3852800
hg1952800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954854
Supporting Variants
SamplesBILGI_BIOE
Known GenesATP13A2, CROCC, MFAP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003141
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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