A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003763



Internal ID19092981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49448439..49522126hg38UCSC Ensembl
Innerchr1:49914111..49987798hg19UCSC Ensembl
Innerchr1:49686698..49760385hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3873688
hg1973688
hg1873688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv163n100
Supporting Variantsnssv3466577
Samples
Known GenesAGBL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003763
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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