A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950610



Internal ID16952797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:36326200..36350399hg38UCSC Ensembl
Outerchr1:36791801..36816000hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3824200
hg1924200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997124
SamplesBILGI_BIOE
Known GenesSTK40
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950610
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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