A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607008



Internal ID16394417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:52941662..53001126hg38UCSC Ensembl
Innerchr7:53009355..53068819hg19UCSC Ensembl
Innerchr7:52976849..53036313hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3859465
hg1959465
hg1859465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1084626
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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