A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690226



Internal ID18988507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39455352..39878557hg38UCSC Ensembl
Innerchr9:41600370..42023575hg19UCSC Ensembl
Innerchr9:41590370..42013575hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38423206
hg19423206
hg18423206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017869
Supporting Variants
Samples
Known GenesKGFLP2, LOC643648, LOC653501, MGC21881
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690226
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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