A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654418



Internal ID18952699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139763000..139979428hg38UCSC Ensembl
Innerchr6:140084137..140300565hg19UCSC Ensembl
Innerchr6:140125830..140342258hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38216429
hg19216429
hg18216429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017015
Supporting Variants
Samples
Known GenesLOC100132735
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654418
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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