A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999785



Internal ID19159321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:771707..863579hg38UCSC Ensembl
Innerchr1:707087..798959hg19UCSC Ensembl
Innerchr1:696950..788822hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3891873
hg1991873
hg1891873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3463004
Samples
Known GenesFAM87B, LINC00115, LINC01128, LOC100288069
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999785
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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