A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960502



Internal ID18860634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16895905..16949205hg38UCSC Ensembl
Outerchr1:17222400..17275700hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3853301
hg1953301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128591
Supporting Variants
SamplesKWS1
Known GenesCROCC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960502
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer