A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005178



Internal ID19094395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61973547..62002981hg38UCSC Ensembl
Innerchr1:62439219..62468653hg19UCSC Ensembl
Innerchr1:62211807..62241241hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3829435
hg1929435
hg1829435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171n100
Supporting Variantsnssv3472565
Samples
Known GenesINADL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005178
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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