A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951993



Internal ID16954180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74124460..74137359hg38UCSC Ensembl
Outerchr15:74416801..74429700hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3812900
hg1912900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999134
SamplesBILGI_BIOE
Known GenesISLR2, LOC283731
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951993
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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