A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550742



Internal ID16338151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46279254hg38UCSC Ensembl
Innerchr10:47543322..47650490hg19UCSC Ensembl
Innerchr10:47013328..47120496hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38107169
hg19107169
hg18107169
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1111n54
Supporting Variantsnssv1173577, nssv1173584, nssv747402, nssv1173585, nssv1173578, nssv1173581, nssv747406, nssv1173575, nssv1173579, nssv747400, nssv747404, nssv747409, nssv1173576, nssv1173580, nssv1173582, nssv747408, nssv1173583, nssv747403, nssv1173586, nssv747401, nssv747407, nssv747405, nssv1173587
SamplesHGDP01087, HGDP00479, HGDP00910, 1780862077_A, HGDP01098, HGDP00913, HGDP00473, 1780862109_A, HGDP00727, HGDP00029, HGDP00472, HGDP00931, HGDP00822
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550742
Frequency
Sample Size17421
Observed Gain13
Observed Loss10
Observed Complex0
Frequencyn/a


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