A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047695



Internal ID18790226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63651743..63689819hg38UCSC Ensembl
Innerchr15:63943942..63982018hg19UCSC Ensembl
Innerchr15:61730995..61769071hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3838077
hg1938077
hg1838077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717951
Samples
Known GenesHERC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047695
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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