A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022906



Internal ID18765440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47670338..47791937hg38UCSC Ensembl
Innerchr7:47709936..47831535hg19UCSC Ensembl
Innerchr7:47676461..47798060hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38121600
hg19121600
hg18121600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6345n100
Supporting Variantsnssv3661250
Samples
Known GenesLINC00525, PKD1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022906
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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