A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014937



Internal ID18757472
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 StatusM
Merged Variants
Supporting Variantsnssv3498236
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)nsv1014937
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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