A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605872



Internal ID16046595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2731265..2737064hg38UCSC Ensembl
Innerchr7:2770899..2776698hg19UCSC Ensembl
Innerchr7:2737425..2743224hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg385800
hg195800
hg185800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078476
Samples
Known GenesGNA12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer