A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020922



Internal ID19110140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77762203..77810979hg38UCSC Ensembl
Innerchr6:78471920..78520696hg19UCSC Ensembl
Innerchr6:78528639..78577415hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3848777
hg1948777
hg1848777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3659057
Samples
Known GenesMEI4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020922
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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