A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018352



Internal ID18760885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26258475..26302205hg38UCSC Ensembl
Innerchr7:26298095..26341825hg19UCSC Ensembl
Innerchr7:26264620..26308350hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3843731
hg1943731
hg1843731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643319
Samples
Known GenesSNX10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018352
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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