A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011197



Internal ID18753731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61973547..61992040hg38UCSC Ensembl
Innerchr1:62439219..62457712hg19UCSC Ensembl
Innerchr1:62211807..62230300hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3818494
hg1918494
hg1818494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv170n100
Supporting Variantsnssv3472039
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)nsv1011197
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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