A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016652



Internal ID19105869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64683570hg38UCSC Ensembl
Innerchr9:69474914..69695988hg19UCSC Ensembl
Innerchr9:68764734..68985808hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38221075
hg19221075
hg18221075
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696109, nssv3696123, nssv3696115, nssv3696117, nssv3696112, nssv3759734, nssv3696121, nssv3696116, nssv3759736, nssv3696114, nssv3696108, nssv3759735, nssv3696120, nssv3696110, nssv3696119, nssv3696122, nssv3759733, nssv3696111, nssv3696118, nssv3696113
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016652
Frequency
Sample Size11257
Observed Gain6
Observed Loss14
Observed Complex0
Frequencyn/a


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