A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3465174



Internal ID18714421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16695774..16932813hg38UCSC Ensembl
Innerchr1:17022269..17259308hg19UCSC Ensembl
Innerchr1:16894856..17131895hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38237040
hg19237040
hg18237040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002740
Supporting Variants
Samples
Known GenesCROCC, ESPNP, LOC729574, 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)nssv3465174
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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