A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv208n100



Internal ID22786295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94660409..94690029hg38UCSC Ensembl
chr1:95125965..95155585hg19UCSC Ensembl
chr1:94898553..94928173hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3829621
hg1929621
hg1829621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009765, nsv1010621, nsv1009168, nsv999580, nsv1004540, nsv1013295, nsv1013150, nsv1014173, nsv1002560, nsv1007625, nsv1011128, nsv1003354, nsv1000399, nsv998738, nsv1004829, nsv1013561, nsv1002928, nsv997636, nsv1001602, nsv1000486, nsv1001354, nsv1012925, nsv1013700
Samples
Known GenesLINC01057
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv208n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss110
Observed Complex0
Frequencyn/a


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