A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034295



Internal ID19123517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7444816..7480778hg38UCSC Ensembl
Innerchr5:7444929..7480891hg19UCSC Ensembl
Innerchr5:7497929..7533891hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3835963
hg1935963
hg1835963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5563n100
Supporting Variantsnssv3746290, nssv3639644
Samples
Known GenesADCY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034295
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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