A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064221



Internal ID19153440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19596411..19631681hg38UCSC Ensembl
Innerchr17:19499724..19534994hg19UCSC Ensembl
Innerchr17:19440316..19475586hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3835271
hg1935271
hg1835271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3117n100
Supporting Variantsnssv3560627, nssv3560628, nssv3560635, nssv3560630, nssv3560650, nssv3560634, nssv3560637, nssv3560636, nssv3719981, nssv3719982, nssv3560646, nssv3560643, nssv3560638, nssv3560632, nssv3560644, nssv3560653, nssv3560639, nssv3560652, nssv3560640, nssv3560633, nssv3560642, nssv3560645, nssv3560629, nssv3560648, nssv3719983, nssv3560631, nssv3560651, nssv3560649, nssv3560641, nssv3560647
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)nsv1064221
Frequency
Sample Size11257
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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