A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3498236



Internal ID18739191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180391765..180430420hg38UCSC Ensembl
Innerchr1:180360900..180399555hg19UCSC Ensembl
Innerchr1:178627523..178666178hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3838656
hg1938656
hg1838656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014937
Supporting Variants
Samples
Known GenesACBD6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3498236
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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