A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017545



Internal ID19106762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188592883..189267889hg38UCSC Ensembl
Innerchr4:189514037..190189043hg19UCSC Ensembl
Innerchr4:189751031..190426037hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38675007
hg19675007
hg18675007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744549
Samples
Known GenesLINC01060
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017545
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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