A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654225



Internal ID18605820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1936627..2280155hg38UCSC Ensembl
Innerchr7:1976263..2319790hg19UCSC Ensembl
Innerchr7:1942789..2286316hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38343529
hg19343528
hg18343528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021310
Supporting Variants
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)nssv3654225
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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