A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026185



Internal ID19115402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19524865..19572623hg38UCSC Ensembl
Innerchr7:19564488..19612246hg19UCSC Ensembl
Innerchr7:19531013..19578771hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3847759
hg1947759
hg1847759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643257, nssv3643258
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026185
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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