A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645227



Internal ID18943508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111142640..111261530hg38UCSC Ensembl
Innerchr7:110782696..110901586hg19UCSC Ensembl
Innerchr7:110569932..110688822hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38118891
hg19118891
hg18118891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025697
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3645227
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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