A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3752803



Internal ID19051084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5666576..5729858hg38UCSC Ensembl
Innerchr7:5706207..5769489hg19UCSC Ensembl
Innerchr7:5672733..5736015hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3863283
hg1963283
hg1863283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028652
Supporting Variants
Samples
Known GenesMIR6874, RNF216, RNF216-IT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3752803
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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