A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018455



Internal ID19107672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61993735hg38UCSC Ensembl
Innerchr9:44727847..45129887hg19UCSC Ensembl
Innerchr9:44667843..45069883hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38473727
hg19402041
hg18402041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7604n100
Supporting Variantsnssv3695588, nssv3695576, nssv3695586, nssv3695578, nssv3695591, nssv3695583, nssv3695589, nssv3695594, nssv3761485, nssv3695581, nssv3695579, nssv3695593, nssv3695587, nssv3695584, nssv3695573, nssv3695590, nssv3695592, nssv3695582, nssv3695580, nssv3695575, nssv3695574, nssv3695585, nssv3695577
Samples
Known GenesFAM27C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018455
Frequency
Sample Size11257
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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