A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021676



Internal ID18764210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152110676..152228495hg38UCSC Ensembl
Innerchr7:151807761..151925580hg19UCSC Ensembl
Innerchr7:151438694..151556513hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38117820
hg19117820
hg18117820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674272
Samples
Known GenesGALNT11, KMT2C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021676
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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