A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031163



Internal ID19120384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17668347..17694130hg38UCSC Ensembl
Innerchr7:17707971..17733754hg19UCSC Ensembl
Innerchr7:17674496..17700279hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3825784
hg1925784
hg1825784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6298n100
Supporting Variantsnssv3643230
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)nsv1031163
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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