A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv39n100



Internal ID19010407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16451184..16965387hg38UCSC Ensembl
chr1:16777679..17291882hg19UCSC Ensembl
chr1:16650266..17164469hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38514204
hg19514204
hg18514204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004738, nsv1000113, nsv1003077, nsv998739, nsv1009669, nsv1000484, nsv1014379, nsv1007741, nsv1003293, nsv1015127, nsv1012519, nsv1002985, nsv1001032, nsv1013089, nsv1002322, nsv1005184, nsv1011657, nsv1004894, nsv1012642, nsv998219, nsv1008783, nsv1014635, nsv1014522, nsv1013995, nsv1011646, nsv1010082, nsv1005297, nsv1005491, nsv1012639, nsv1012031, nsv1001569, nsv1005562
Samples
Known GenesCROCC, CROCCP2, CROCCP3, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1, NECAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv39n100
Frequency
Sample Size29084
Observed Gain50
Observed Loss0
Observed Complex0
Frequencyn/a


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