A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009765



Internal ID19098984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94687282hg38UCSC Ensembl
Innerchr1:95130666..95152838hg19UCSC Ensembl
Innerchr1:94903254..94925426hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3822173
hg1922173
hg1822173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3480298, nssv3467988, nssv3467993, nssv3470308, nssv3465499, nssv3463443, nssv3468557, nssv3471551, nssv3482158, nssv3474915, nssv3466076, nssv3480009, nssv3466385, nssv3474984, nssv3480292, nssv3464643, nssv3477923, nssv3476389, nssv3478144, nssv3477359, nssv3478680, nssv3473259, nssv3468527, nssv3478438, nssv3474452, nssv3467835, nssv3463839, nssv3472194, nssv3479385, nssv3468125, nssv3463844, nssv3472114, nssv3475001, nssv3479070, nssv3463068, nssv3468680, nssv3478857, nssv3473961, nssv3469223
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)nsv1009765
Frequency
Sample Size11257
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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