A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951004



Internal ID16953191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:101820544..101835543hg38UCSC Ensembl
Outerchr10:103580301..103595300hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3815000
hg1915000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998036
SamplesBILGI_BIOE
Known GenesKCNIP2, KCNIP2-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951004
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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