A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015245



Internal ID19104462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20149138..20203859hg38UCSC Ensembl
Innerchr7:20188761..20243482hg19UCSC Ensembl
Innerchr7:20155286..20210007hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3854722
hg1954722
hg1854722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643266
Samples
Known GenesMACC1, MACC1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015245
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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