A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013309



Internal ID19102527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269902..25320443hg38UCSC Ensembl
Innerchr1:25596393..25646934hg19UCSC Ensembl
Innerchr1:25468980..25519521hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3850542
hg1950542
hg1850542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv139n100
Supporting Variantsnssv3474491, nssv3476122, nssv3468835, nssv3471554, nssv3464778, nssv3479865, nssv3481606, nssv3482706, nssv3482074, nssv3463993, nssv3481144, nssv3472227, nssv3476161, nssv3470034, nssv3474173
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013309
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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