A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027123



Internal ID19116342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7830416..7886657hg38UCSC Ensembl
Innerchr7:7870047..7926288hg19UCSC Ensembl
Innerchr7:7836572..7892813hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3856242
hg1956242
hg1856242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655109
Samples
Known GenesRPA3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027123
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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