A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641186



Internal ID18939467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139751798..139855709hg38UCSC Ensembl
Innerchr4:140672952..140776863hg19UCSC Ensembl
Innerchr4:140892402..140996313hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38103912
hg19103912
hg18103912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019522
Supporting Variants
Samples
Known GenesMAML3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3641186
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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