A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696750



Internal ID18648345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:356431..1003629hg19UCSC Ensembl
Innerchr1:346294..993492hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg19647199
hg18647199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002919
Supporting Variants
Samples
Known GenesAGRN, C1orf170, FAM41C, FAM87B, HES4, ISG15, KLHL17, LINC00115, LINC01128, LOC100130417, LOC100133331, LOC100288069, MIR6723, NOC2L, OR4F16, OR4F29, OR4F3, PLEKHN1, SAMD11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696750
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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