A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127122



Internal ID18915731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71759398..71759464hg38UCSC Ensembl
Outerchr10:73519155..73519221hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985477
SamplesKWS1
Known GenesC10orf54, CDH23
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127122
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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