A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056853



Internal ID19146072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19598630..19635122hg38UCSC Ensembl
Innerchr17:19501943..19538435hg19UCSC Ensembl
Innerchr17:19442535..19479027hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3836493
hg1936493
hg1836493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3117n100
Supporting Variantsnssv3560898, nssv3560896, nssv3560900, nssv3560895, nssv3560897, nssv3560899, nssv3720016, nssv3720017, nssv3560901, nssv3560894
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056853
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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