A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027945



Internal ID19117163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3085878..3168438hg38UCSC Ensembl
Innerchr7:3125512..3208071hg19UCSC Ensembl
Innerchr7:3092038..3174597hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3882561
hg1982560
hg1882560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6221n100
Supporting Variantsnssv3654233
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)nsv1027945
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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