A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949935



Internal ID16952122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:124762247..124767246hg38UCSC Ensembl
Outerchr7:124402301..124407300hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998576
SamplesBILGI_BIOE
Known GenesGPR37
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949935
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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