A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3698864



Internal ID18650459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16559628..16935740hg38UCSC Ensembl
Innerchr1:16886123..17262235hg19UCSC Ensembl
Innerchr1:16758710..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38376113
hg19376113
hg18376113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012639
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)nssv3698864
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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