A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018250



Internal ID19107467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15609236..15628257hg38UCSC Ensembl
Innerchr7:15648861..15667882hg19UCSC Ensembl
Innerchr7:15615386..15634407hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3819022
hg1919022
hg1819022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643184
Samples
Known GenesMEOX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018250
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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