A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3659057



Internal ID18957338
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 StatusS
Merged Variantsnsv1020922
Supporting Variants
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)nssv3659057
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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