A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054574



Internal ID18797105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103210111..105365114hg38UCSC Ensembl
Innerchr14:103676448..105831451hg19UCSC Ensembl
Innerchr14:102746201..104902496hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382155004
hg192155004
hg182156296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3711393
Samples
Known GenesADSSL1, AHNAK2, AKT1, APOPT1, ASPG, BAG5, BRF1, BTBD6, C14orf180, C14orf2, C14orf79, CDCA4, CEP170B, CKB, EIF5, GPR132, INF2, JAG2, KIF26A, KLC1, LINC00637, LINC00638, MARK3, MIR203, MIR3545, MIR4710, MIR6765, NUDT14, PACS2, PLD4, PPP1R13B, RD3L, SIVA1, SNORA28, TDRD9, TMEM179, TRMT61A, XRCC3, ZBTB42, ZFYVE21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054574
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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