A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111805



Internal ID19280203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:51070162..51156062hg38UCSC Ensembl
Outerchr2:51297300..51383200hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3885901
hg1985901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n106
Supporting Variantsnssv3964715
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111805
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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