A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955792



Internal ID16957979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:152068861..152071099hg38UCSC Ensembl
Outerchr6:152389996..152392234hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382239
hg192239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002284
SamplesBILGI_BIOE
Known GenesESR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955792
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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