A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002864



Internal ID18745396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24763019..24796249hg38UCSC Ensembl
Innerchr1:25089510..25122740hg19UCSC Ensembl
Innerchr1:24962097..24995327hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3833231
hg1933231
hg1833231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3465288
Samples
Known GenesCLIC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002864
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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