A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024183



Internal ID19113400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116287872..116314039hg38UCSC Ensembl
Innerchr7:115927926..115954093hg19UCSC Ensembl
Innerchr7:115715162..115741329hg18UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3826168
hg1926168
hg1826168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6592n100
Supporting Variantsnssv3662047
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)nsv1024183
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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