A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013089



Internal ID18755620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16559628..16965387hg38UCSC Ensembl
Innerchr1:16886123..17291882hg19UCSC Ensembl
Innerchr1:16758710..17164469hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38405760
hg19405760
hg18405760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv39n100
Supporting Variantsnssv3475510
Samples
Known GenesCROCC, CROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013089
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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