A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766021



Internal ID18962474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16555304..16674305hg38UCSC Ensembl
chr1:16881799..17000800hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38119002
hg19119002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077283
Supporting Variants
SamplesKWP1
Known GenesCROCCP2, LOC729574, MST1P2, NBPF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766021
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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