A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604902



Internal ID16045625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152069044..152071039hg38UCSC Ensembl
Innerchr6:152390179..152392174hg19UCSC Ensembl
Innerchr6:152431872..152433867hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381996
hg191996
hg181996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10970n54
Supporting Variantsnssv1074577, nssv1074572, nssv1074576, nssv1074573, nssv1074578, nssv1074574, nssv1074575
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604902
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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