A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3463161



Internal ID18713346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16596505..16695774hg38UCSC Ensembl
Innerchr1:16923000..17022269hg19UCSC Ensembl
Innerchr1:16795587..16894856hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3899270
hg1999270
hg1899270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001891
Supporting Variants
Samples
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, 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)nssv3463161
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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