A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003274



Internal ID18745806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16691023..16988207hg38UCSC Ensembl
Innerchr1:17017518..17314702hg19UCSC Ensembl
Innerchr1:16890105..17187289hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38297185
hg19297185
hg18297185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv92n100
Supporting Variantsnssv3469037
Samples
Known GenesATP13A2, CROCC, ESPNP, LOC729574, MFAP2, MIR3675, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003274
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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