A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607976



Internal ID16048699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101160859..101238359hg38UCSC Ensembl
Innerchr7:100804140..100881640hg19UCSC Ensembl
Innerchr7:100590860..100668360hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3877501
hg1977501
hg1877501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11534n54
Supporting Variantsnssv1091887
Samples
Known GenesAP1S1, CLDN15, MOGAT3, NAT16, PLOD3, VGF, ZNHIT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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