A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004202



Internal ID18746733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16864355..16931176hg38UCSC Ensembl
Innerchr1:17190850..17257671hg19UCSC Ensembl
Innerchr1:17063437..17130258hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3866822
hg1966822
hg1866822
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n100
Supporting Variantsnssv3474550, nssv3481061, nssv3474924, nssv3474762, nssv3462849, nssv3465398, nssv3477896, nssv3468772, nssv3467537, nssv3476089, nssv3481008, nssv3482092, nssv3463026, nssv3482012, nssv3471343, nssv3477305
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004202
Frequency
Sample Size29084
Observed Gain5
Observed Loss11
Observed Complex0
Frequencyn/a


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