A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083837



Internal ID15590337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:49632287..50387038hg38UCSC Ensembl
Innerchr7:49671883..50454736hg19UCSC Ensembl
Innerchr7:49642429..50422230hg18UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38754752
hg19782854
hg18779802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606897
Supporting Variants
Samples
Known GenesC7orf72, IKZF1, VWC2, ZPBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083837
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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