A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635995



Internal ID18934276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29125695..29204079hg38UCSC Ensembl
Innerchr5:29125802..29204186hg19UCSC Ensembl
Innerchr5:29161559..29239943hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3878385
hg1978385
hg1878385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030526
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635995
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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