A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152677



Internal ID15881002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:45173674..45263029hg38UCSC Ensembl
Innerchr4:45175691..45265046hg19UCSC Ensembl
Innerchr4:44870448..44959803hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3889356
hg1989356
hg1889356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594105
Supporting Variants
SamplesNINDS_58
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152677
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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