A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003129



Internal ID16949395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:15931306..15953205hg38UCSC Ensembl
Outerchr1:16257801..16279700hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821900
hg1921900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954843
Supporting Variants
SamplesBILGI_BIOE
Known GenesSPEN, ZBTB17
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003129
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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