A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011696



Internal ID18754230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16599641..16710590hg38UCSC Ensembl
Innerchr1:16926136..17037085hg19UCSC Ensembl
Innerchr1:16798723..16909672hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38110950
hg19110950
hg18110950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv66n100
Supporting Variantsnssv3471722
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)nsv1011696
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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