A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122975



Internal ID19278053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64184111..64184177hg38UCSC Ensembl
Outerchr15:64476310..64476376hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971571
SamplesKWS2
Known GenesCSNK1G1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122975
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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