A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3698796



Internal ID18650391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16518425..16876990hg38UCSC Ensembl
Innerchr1:16844920..17203485hg19UCSC Ensembl
Innerchr1:16717507..17076072hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38358566
hg19358566
hg18358566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002985
Supporting Variants
Samples
Known GenesCROCCP2, 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)nssv3698796
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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