A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951640



Internal ID16953827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:44842002..44848101hg38UCSC Ensembl
Outerchr7:44881601..44887700hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997642
SamplesBILGI_BIOE
Known GenesH2AFV
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951640
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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