A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036200



Internal ID18778731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30350881..30488448hg38UCSC Ensembl
Innerchr15:30643084..30780651hg19UCSC Ensembl
Innerchr15:28430376..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38137568
hg19137568
hg18137568
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2522n100
Supporting Variantsnssv3546784, nssv3546785
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036200
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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