A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025961



Internal ID18768493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31480756..31530058hg38UCSC Ensembl
Innerchr6:31448533..31497835hg19UCSC Ensembl
Innerchr6:31556512..31605814hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3849303
hg1949303
hg1849303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745373
Samples
Known GenesMCCD1, MICB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025961
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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