A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951639



Internal ID16953826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:44753502..44769501hg38UCSC Ensembl
Outerchr7:44793101..44809100hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3816000
hg1916000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997641
SamplesBILGI_BIOE
Known GenesZMIZ2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951639
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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