A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021173



Internal ID18763707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2206456..2334992hg38UCSC Ensembl
Innerchr7:2246091..2374627hg19UCSC Ensembl
Innerchr7:2212617..2341153hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38128537
hg19128537
hg18128537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654226
Samples
Known GenesFTSJ2, MAD1L1, MIR6836, NUDT1, SNX8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021173
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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