A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639136



Internal ID18937417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81724904..82123459hg38UCSC Ensembl
Innerchr5:81020723..81419278hg19UCSC Ensembl
Innerchr5:81056479..81455034hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38398556
hg19398556
hg18398556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028322
Supporting Variants
Samples
Known GenesATG10, SSBP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639136
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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