A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645772



Internal ID18944053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:100298059..100513939hg38UCSC Ensembl
Innerchr5:99633763..99849643hg19UCSC Ensembl
Innerchr5:99661662..99877542hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38215881
hg19215881
hg18215881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019588
Supporting Variants
Samples
Known GenesLOC100133050
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3645772
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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