A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137862



Internal ID18906645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1011052..1011138hg38UCSC Ensembl
Outerchr10:1056992..1057078hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990383
SamplesKWS2
Known GenesGTPBP4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137862
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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