A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466238



Internal ID18714965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16949734hg38UCSC Ensembl
Innerchr1:16871266..17276229hg19UCSC Ensembl
Innerchr1:16743853..17148816hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38404964
hg19404964
hg18404964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006011
Supporting Variants
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)nssv3466238
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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