A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111930



Internal ID19273421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64340979..64341304hg38UCSC Ensembl
Outerchr15:64633178..64633503hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1223n106
Supporting Variantsnssv3964849
SamplesKWS2
Known GenesCSNK1G1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111930
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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