A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661463



Internal ID18959744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56740039..57001021hg38UCSC Ensembl
Innerchr7:56807732..57068728hg19UCSC Ensembl
Innerchr7:56775226..57072670hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38260983
hg19260997
hg18297445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019894
Supporting Variants
Samples
Known GenesLOC100130849, MIR4283-1, MIR4283-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661463
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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